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Aberto até de Madrugada: Airbus faz 1ª descolagem totalmente automática   


A Airbus fez esta semana a demonstração de uma descolagem feita de forma completamente automática, sem intervenção dos pilotos a bordo.

A Airbus concluiu com sucesso a primeira descolagem automática com base na visão, usando um avião de testes Airbus no aeroporto Toulouse-Blagnac. A tripulação de testes, composta por dois pilotos e três engenheiros de voo, fez a 1ª descolagem às 10h15 do dia 18 de Dezembro e realizou um total de 8 descolagens num período de quatro horas e meia. Este marco histórico para a pesquisa aeronáutica foi comunicado apenas esta semana pela Airbus.

A descolagem automática é um marco importante no projecto ATTOL (Autonomous Taxi, Take-Off & Landing) da Airbus. Lançado em Junho de 2018, o ATTOL é uma das demonstrações tecnológicas de voo que a Airbus tem vindo a testar, com o objectivo de compreender o impacto da automatização e autonomia nos aviões. A Airbus não encara a autonomia como uma meta em si, mas sim como uma forma de explorar tecnologias em conjunto com outras inovações em áreas como materiais, electrificação e conectividade.

Para que as tecnologias de automatização melhorem os voos e a performance geral dos aviões, os pilotos terão que continuar no centro das operações. As tecnologias autónomas são fundamentais para apoiar os pilotos, permitindo-lhes concentrarem-se menos na operação das aeronaves e mais na tomada de decisões estratégicas e na gestão do vôo.


Altalube (Altaire Pharmaceuticals Inc.)   


As a lubricant to prevent further irritation, to relieve dryness of the eye(s). Warnings: For use in the eyes only. Save box for complete information. When using this product: avoid…


Multi-Action Relief (Altaire Pharmaceuticals Inc.)   


For the temporary relief of burning and irritation due to dryness of the eye, for use as a protectant against further irritation or to relieve dryness of the eye, relieves redness of the…


Altachlore Sodium Chloride Hypertonicity (Altaire Pharmaceuticals Inc.)   


For the temporary relief of corneal edema. Warnings: For use in the eyes only Save box for complete information. Do not use except under the advice and supervision of a doctor, if…


High Court Won't Hear Dispute Over Patented Schizophrenia Drug   

WASHINGTON, D.C. - In its Jan. 13 order list, the U.S. Supreme Court rejected a petition for certiorari that poses the question of whether method-of-treatment patent claims automatically satisfy Section 101 of the Patent Act, even if they consist only of application of natural law using routine steps (Hikma Pharmaceuticals USA Inc., et al. v. Vanda Pharmaceuticals USA Inc., No. 18-817, U.S. Sup.).

In Sensipar Patent Row, Federal Circuit Vacates Noninfringement Holding   

WASHINGTON, D.C. - A Delaware federal judge's incorrect claim construction led to an erroneous finding of noninfringement, the Federal Circuit U.S. Court of Appeals held Jan. 7 in a win for patent owner Amgen Inc., maker of the drug "Sensipar" (Amgen Inc. v. Amneal Pharmaceuticals LLC, et al., Nos. 2018-2414, 2019-1086, Fed. Cir., 2020 U.S. App. LEXIS 245).

Is Your Food Grown on Sewage?   


If you've never heard of sewage sludge — a term often used interchangeably with biosolids — you're in for a surprise, as this waste product, which is every bit as unappealing as it sounds, is applied to farmland, gardens, schoolyards, lawns and more across the U.S. The food you eat may very well have come from land treated with sewage sludge, which could have implications for human health and the environment.

What exactly is sewage sludge? When wastewater and stormwater enter wastewater treatment facilities, the solid and liquid waste are separated. The solids are "digested" using bacteria, treated, dried and then sent to landfills or used for agricultural purposes as "fertilizer."

It may sound shocking, but this practice is allowed and endorsed by the U.S. EPA. It's not only legal but routine to grow food on sewage sludge-treated land, even though the sludge, by definition, can contain any number of toxic chemicals that may not be removed via treatment. The Center for Food Safety explained:1

"These separated processed solids — sewage sludge — contain numerous known and unknown hazardous materials.

This includes everything that is flushed into the sewer system, including: household, medical, chemical, and industrial waste; chemicals and metals that leach from the sewer pipes themselves; and novel materials that are created in the wastewater treatment plant as a result of the combination of chemicals and organic compounds present."

Applying Sewage Waste to Soil 'Defies Common Sense'

In the U.S., 54% of sewage sludge biosolids are used for so-called "beneficial" purposes. Most often this means they're applied to agricultural sites, although small amounts are also applied to forestry sites and reclamation sites, including Superfund and Brownfield lands and urban areas, including park land.

Broken down, it's estimated that 36% of biosolids are used for agricultural purposes while 28% end up in landfills and 15% are incinerated.2

The fact is, humans produce a healthy amount of waste — an estimated 300 million pounds of feces are produced daily by Americans alone, for instance. How to dispose of this biosolid sludge is a vexing problem worldwide, so theoretically, turning the waste product into a beneficial product like fertilizer makes sense, assuming it could be thoroughly purified.

Therein lies the problem, however. The Guardian quoted former EPA scientist David Lewis, who opposed the use of sewage sludge on cropland. Lewis noted, "Spending billions of dollars to remove hazardous chemicals and biological wastes from water, only to spread them on soil everywhere we live, work and play defies common sense."3

While it's true that sewage sludge contains similar ingredients to synthetic fertilizer, such as nitrogen and phosphorus, it also contains countless other pollutants that are byproducts of modern-day life. As noted by The Guardian:4

" … [T]he excrement from which sludge derives has mixed with any number of 80,000 manmade chemicals that are discharged from industry's pipes or otherwise pumped into the sewer system.

By the time the mix lands in treatment plants, it can teem with pharmaceuticals, hormones, pathogens, bacteria, viruses, protozoa and parasitic worms, as well as heavy metals like lead, cadmium, arsenic or mercury. It often includes PCBs, PFAS, dioxins, BPAs and dozens of other harmful substances ranging from flame retardants to hospital waste."

It's worth noting that while sewage sludge used to be disposed of primarily by burning it or releasing it into the ocean, this practice was banned over concerns that it would pollute the air and water. But spreading it onto soil has somehow received a safety approval from regulatory agencies,5 including the EPA, which describes them as purely beneficial:6

"They [biosolids] are nutrient-rich organic materials resulting from the treatment of domestic sewage in a treatment facility. When treated and processed, these residuals can be recycled and applied as fertilizer to improve and maintain productive soils and stimulate plant growth."

EPA Identified 352 Pollutants in Sewage Sludge

As part of the Clean Water Act, the EPA must review biosolids standards every two years. Technically speaking, the EPA refers to sewage sludge that has gone through treatment and meets EPA standards for land application as "biosolids."

Part of the review includes identifying pollutants that are present. Based on these biennial reviews and three national sewage sludge surveys, the EPA identified 352 pollutants in biosolids,7 including the following:8


Dioxins and dioxin-like compounds

Inorganic ions

Certain organics (i.e., polycyclic aromatic hydrocarbons, semivolatiles)

Polybrominated diphenyl ethers (flame retardants)


Steroids and hormones

Per- and polyfluoroalkyl substances

In a report from the U.S. Office of Inspector General (OIG) released November 2018, it's concluded that the EPA is unable to assess the impact of the hundreds of unregulated pollutants applied to land via biosolids on human health and the environment.9

The report was the result of an audit conducted by OIG to determine whether the EPA has controls over the application of biosolids to land in order to protect human and environmental health.

OIG concluded that the EPA "lacked the data or risk assessment tools needed to make a determination on the safety of 352 pollutants found in biosolids" and noted that 61 of the identified pollutants are "acutely hazardous, hazardous or priority pollutants in other programs."10

EPA Biosolids Program Not Protecting Public Health

Further, while the EPA could conduct full risk assessments to gauge biosolids risks, it is not required to do so. Overall, OIG found that the EPA biosolids program was likely not protecting public health and the environment:11

"The EPA has reduced staff and resources in the biosolids program over time, creating barriers to addressing control weaknesses identified in the program.

Past reviews showed that the EPA needed more information to fully examine the health effects and ecological impacts of land-applied biosolids. Although the EPA could obtain additional data to complete biosolids risk assessments, it is not required to do so.

Without such data, the agency cannot determine whether biosolids pollutants with incomplete risk assessments are safe. The EPA's website, public documents and biosolids labels do not explain the full spectrum of pollutants in biosolids and the uncertainty regarding their safety.

Consequently, the biosolids program is at risk of not achieving its goal to protect public health and the environment."

Research from the U.S. Geological Survey (USGS) has also shown household chemicals and drugs are found in biosolids originating from wastewater treatment plants.12 The researchers purchased or obtained nine different biosolids and analyzed them for 87 organic chemicals, finding 55 were detected in measurable amounts and as many as 45 were found in a single sample.

Plastics in Sewage Sludge

Researchers have also looked into how polyester microfibers may be affecting microorganisms in the soil, especially since sewage sludge is loaded with microfibers.13 They found that the microplastics did, indeed, lead to changes in the soil, including altering the bulk density, water-holding capacity and microbial activity.

Writing in the journal Environmental Science & Technology, researchers noted that wastewater treatment plants act as receptors for the "cumulative loading of microplastics." The solids and liquids are separated using a settlement process, which results in the majority of microplastics (MP ending up in sewage sludge.

Different methods of treatment affected the end number of particles found in the sludge, but the study found microplastic amounts ranging from 4,196 to 15,385 particles kg–1 (dry weight) in sludge samples.14

The researchers noted, "This study highlights the potential for sewage sludge treatment processes to affect the risk of MP pollution prior to land spreading and may have implications for legislation governing the application of biosolids to agricultural land."

Microplastics may act like sponges for contaminants including heavy metals, persistent organic pollutants, polychlorinated biphenyls (PCBs) or pathogens, for instance, and may cause harm on a cellular or subcellular level,15 raising serious questions about the risks of exposing soil to them.

Indeed, wastewater treatment plants are efficient at removing microplastics from sewage, but they become trapped in the sludge. This helps keep them out of waterways, unless they're applied to agricultural soils (which may run off into waterways).

When researchers evaluated 31 fields that had applications of sewage sludge, microplastics were found in the samples at levels ranging from 18 to 41 particles g−1, with a median of 34 particles g−1.16 What's more, the microplastic levels increased on fields with higher rates of sludge applications.

"Our results indicate that microplastic counts increase over time where successive sludge applications are performed," the researchers noted, adding, "Sludge is proposed as a primal driver of soil microplastic pollution."17

Sewage Sludge Contaminating Farms

Sewage sludge is passed off as a cost-effective fertilizer for farmers, but some have lost their livelihoods after the toxic waste contaminated their farms. One such farmer is Fred Stone in Maine, who applied biosolids to his hayfields intended to feed his dairy cattle for decades, not knowing it could be contaminated with PFAS, chemicals associated with cancer, liver damage, low birth weight and hypothyroidism.

Milk from Stone's cows later tested positive for PFAS, forcing him to dump hundreds of gallons of milk a day.18 In March 2019, the Maine Department of Environmental Protection added a requirement to test sewage sludge for PFAS before it's applied to land.19

This is just the tip of the iceberg, as long-term application of sewage sludge also increases the abundance and diversity of antibiotic resistance genes in soil.20 In a study from the University of York in the United Kingdom, data even revealed plants suffer when biosolids are applied to the soil.21

Even with low-level exposure, the drugs studied interfered with plant hormones that support defense against predators and diseases. The drugs also damaged the plants' ability to make energy from sunlight, and at higher concentrations the research team saw a drop in the leaves' levels of chlorophyll. At high concentrations, the plants experienced stunted roots and burnt edges on the leaves.

How to Avoid Biosolids

Foods grown on biosolid-treated soil are not labeled as such, so your best bet for avoiding them is to support sustainable agriculture movements in your area. Make it a point to only buy food from a source you know and trust — one using safe, nontoxic organic or biodynamic farming methods.

If you grow your own food, also be aware that companies do not have to disclose when biosolids are used, so there's really no way of knowing what's in your bag of potting soil or compost. Composted products can have the USDA organic label on them and still be loaded with toxic biosolids.

If you see "milogranite" on the label, it contains biosolids from the City of Milwaukee — a national distributor. Your best bet is to buy organic potting soil and/or compost from a local nursery you know and trust, that can guarantee no biosolids have been added.


Mandatory Flu Vaccine Coming Your Way?   


As discussed in my November 5, 2019, article, “Trojan Horse of Measles — More Vaccines With the Mandate,” while most state legislation targeting vaccination mandates have focused on measles, what tends to get lost in the debate is that these mandatory vaccination laws are likely to be extended to all vaccines, including the influenza vaccine, the human papillomavirus (HPV) vaccine and any number of vaccines licensed and recommended by the federal government in the future.

In other words, measles outbreaks and the fear-mongering by exaggerating disease risks and minimizing vaccine risks are being cleverly used to create propaganda to eliminate the legal right to make vaccine choices across the board. As just one example, in “Trojan Horse of Measles,” I discuss how a bill has been introduced in New York that requires children to be vaccinated against HPV in order to attend day care and public school.

This, despite the incredible health risks associated with the HPV vaccine and its low benefit-to-risk ratio,1 not to mention the fact that it has never been proven to lower cancer rates. On the contrary, emerging data suggest the incidence of cervical cancer increased in Sweden after HPV vaccine was recommended for all girls and women aged 9 to 26 years.

Scientific evidence of an increase in the incidence of HPV-related cervical cancer in Sweden between 2006 and 20152 was published in the Indian Journal of Medical Ethics in 2018. The study raised questions about whether women are at increased risk for cervical cancer if they are vaccinated after they have been infected with HPV, which is an asymptomatic viral infection that is cleared from the body within two years by more than 90 percent of women and men.3

The study was retracted a few weeks after it was published. The retraction was not due to falsification of data, but because the scientist who wrote the study used a pseudonym and false affiliation due to fear he would be harmed for publishing his findings. As explained in the retraction statement by the publisher:4

“On inquiry, the author informed us that he had used a pseudonym besides a false affiliation. He later made his identity known to IJME’s editor on the promise of strict confidentiality.

On verification of his identity, the editor confirmed that (a) the author had the necessary qualifications, expertise and research experience on the subject of the article; and (b) the author did face a credible threat of harm, making it necessary not to be named publicly.

Further we reconfirmed the reviewers’ conclusions: that the article used publicly available data with a simple statistical method; made a fair attempt to report a possible association of the increased incidence of carcinoma cervix with HPV vaccination …

We felt that the data and analysis could be scientifically appreciated and critiqued without reference to the author … Following our decision, we received valuable advice from our editorial board and other well-wishers, emphasizing that there should be zero tolerance to the author’s deception, irrespective of the content of the paper.

While our assessment of the science of the article may be correct, we have concluded that tolerating the author’s deception and retaining the article was an error of judgment. … We hope that the hypothesis of possible harm of vaccinating women previously exposed to HPV is carefully explored in future studies.”

Chairman and chief legal counsel for Children's Health Defense Robert F. Kennedy Jr. stated in “The Plaintiff’s Science Day Presentation on Gardasil,” that Merck’s HPV vaccine Gardasil “has distinguished itself as the most dangerous vaccine ever invented."

In his presentation, Kennedy reveals Merck data showing Gardasil increases the overall risk of death by 370%, risk of autoimmune disease by 2.3% and risk of a serious medical condition by 50%.

A 2018 study published in the Journal of Toxicology and Environmental Health5 found that women who received HPV vaccinations suffered higher rates of infertility. According to this study, “if 100% of females in this study had received the HPV vaccine, data suggest the number of women having ever conceived would have fallen by 2 million."

After “skeptic” critics of scientific evidence that vaccines have significant health risks publicly attacked the study, the paper was withdrawn by the publisher.6

A 2014 case report paper7 described cases of three adolescent girls who suffered premature ovarian insufficiency after their HPV vaccinations — a condition that can render them incapable of bearing children in the future. Conveniently, Merck, maker of Gardasil, is also “the world market leader in fertility treatments,” according to the European Pharmaceutical Review.8

Media and Public Health Agencies Are Letting Us Down

Unfortunately, our media no longer fulfill their public duty. Rather than presenting both sides of an argument, most mainstream media now act as mouthpieces for pharmaceutical industry propaganda, and this is particularly true where vaccines are concerned.

Public health agencies are also falling short of their duty, the U.S. Centers for Disease Control and Prevention included, which for years has lied about accepting funds from corporations making and selling drugs and vaccines.

Several watchdog groups are now petitioning the CDC to cease making false disclaimers about not accepting commercial support, and to retroactively acknowledge conflicts of interest.

Another lawsuit, filed by the Informed Consent Action Network (ICAN) in 2018 against the U.S. Department of Health and Human Services, revealed the HHS — in violation of federal law — has not provided a single required biannual vaccine safety report to Congress since 1988.9 As noted by ICAN founder Del Bigtree:10

"It is apparent that HHS doesn't have a clue as to the actual safety profile of the now 39 doses, and growing, of vaccines given by one year of age, including in utero. In 1986, a one-year old child received 11 doses.

HHS spends billions annually promoting vaccines and generates a steady stream of reports promoting vaccines. Yet, when, despite federal law, HHS cannot bother to complete the simple task of preparing a biennial report on vaccine safety, there is little hope HHS is tackling the much harder job of improving vaccine safety."

Vaccine Science Is Not Being Reported Honestly

A 2018 article11 in The BMJ highlights the media’s influence over vaccine policy and how journalists are misleading the public about vaccine safety and effectiveness. The article, “Reporting Flu Vaccine Science,” written by freelance journalist Rob Wipond, notes:

When reporting on medical studies, the popular press has a habit of sensationalizing. So the muted response to a recent research paper12 reporting increased risk of miscarriage with influenza vaccines was at first sight surprising.

The study, funded by the Centers for Disease Control and Prevention, found that women who had received an influenza vaccine containing the 2009 pandemic strain pH1N1 and who were also vaccinated in the next flu season had a statistically significant, 7.7-fold higher odds of spontaneous abortion within 28 days of the second vaccination …

The concerning odds ratio fostered extensive discussion in the paper. But the news media projected an air of calm, highlighting the observational study’s many limitations.”

Among the “muted” press coverage cited by Wipond is The Washington Post’s report13 on the study, written by Lena Sun, which significantly downplayed the findings and urged pregnant women to continue getting their annual flu shot.

This isn’t surprising considering Sun was one of three journalists hand-selected by the CDC to get exclusive early access to the findings, knowing she could be trusted to report on the study in a way that would minimize influenza vaccine risks so pregnant women would be persuaded to get a flu shot during every pregnancy.14,15

Hypocrisy and Double Standards

In a reply to Wipond’s article, retired pediatrician Allan S. Cunningham seconds many of Wipond’s concerns, stating:16

“After weeks of brooding about the Donahue article linking flu shots to miscarriages … it was with a sense of relief that I read Rob Wipond’s narrative of media attempts to sweep a serious vaccine safety issue under the rug.

He points out the hypocrisy (his words were ‘double standard’) of authorities who dismissed the Donahue paper because it was an ‘observational study.’ Year after year they have quoted observational studies to announce, ‘ … 80% vaccine effectiveness … 60% effectiveness … 40% effectiveness …’

They do not mention that these studies make no effort to look for adverse vaccine effects (e.g. narcolepsy, seizures, high fever, oculorespiratory syndrome). They do not mention ‘negative vaccine effectiveness,’ the increase in risk of illness from influenza and non-influenza viruses associated with (or caused by) the vaccines …

They do not mention that a vaccine ‘effective’ in one season may increase influenza risk in a subsequent season … They do not mention that the observational studies they refer to are likely to exaggerate vaccine effectiveness in the first place because of the ‘healthy user effect’ well known to epidemiologists …

Wipond does not mention another technique used to dismiss legitimate vaccine safety concerns, having to do with ‘statistical significance.’ Recently, a large cohort study17 found that flu shots given during the first trimester of pregnancy were associated with a 20% increase in autism spectrum disorder in the offspring.

P for the association was 0.01, and the authors acknowledged that, if it was causal, would mean four (4) additional autism cases for every 1,000 mothers vaccinated.

However, they incorrectly used a statistical manipulation to adjust the finding into ‘non-significance’ … One typical media headline about the study was, ‘Flu vaccine during pregnancy not linked to autism’ … This kind of thing goes on all the time with news releases for vaccine research.”

Why You Cannot Trust The Washington Post

Washington Post reporter Lena Sun has published a number of patently false claims about vaccines,18 and has attacked me personally for making fully referenced and scientifically provable statements about vaccine risks and the fact that maintaining adequate vitamin D levels has been shown to be effective in preventing respiratory infections, even more effective than the flu vaccine.

In a November 21, 2019, article,19 journalist Jeremy Hammond details four instances that exemplify how Sun has lied about vaccine safety. To repeat but one, Sun has stated that:20

“The effectiveness of the vaccine schedule is tested extensively to ensure that the vaccines in the combination don’t interfere with one another and can be easily handled by the infant and the child’s immune system. No new immunization is added to the schedule until it has been evaluated both alone and when given with the other current immunizations.”

As noted by Hammond, this is “a brazen lie,” as published papers21 and even committees at the Institute of Medicine22 (which the CDC considers an authoritative source) have warned about the complete lack of such testing, and the fact that there not only is inadequate scientific evidence to prove safety of the CDC’s birth to age 6 childhood vaccination schedule, but that the synergistic effects of giving multiple vaccines to infants and children has not been adequately studied.

Flu Vaccination Increases Risk of Pandemic Flu

New York, New Jersey and other states have introduced bills to mandate Influenza vaccines for children and adults,23 while the mainstream media continues to ignore evidence that routine flu vaccination increases risks for influenza infections during pandemic outbreaks. A study24 published in the Journal of Virology in 2011 pointed out that:

“Infection with seasonal influenza A viruses induces immunity to potentially pandemic influenza A viruses of other subtypes (heterosubtypic immunity).”

And that “long-term annual vaccination using inactivated vaccines may hamper the induction of cross-reactive CD8+ T cell responses by natural infections and thus may affect the induction of heterosubtypic immunity.”

The study’s authors note that long-term annual vaccination, in turn, “may render young children who have not previously been infected with an influenza virus more susceptible to infection with a pandemic influenza virus of a novel subtype.”

In simpler terms, while naturally experiencing and recovering from type A influenza can provide immunity against other subtypes of the influenza virus, it appears that vaccination does not do that, making previously vaccinated children more susceptible to pandemic flu strains. (Pandemic influenza is when a new influenza A virus appears that spreads easily among individuals and spreads globally.25)

Other studies linking annual flu vaccination with increased risk of illness are listed in my March 2019 article “Is the Flu Vaccine Really ‘Working Well’ This Year?

Influenza Vaccine Is Vastly Oversold

Mainstream media outlets also will not admit that Pharma bias compromises the results of most vaccine studies. Yet the presence of such bias was clearly highlighted in a 2010 study26 by the Cochrane Database of Systemic Reviews, in which they assessed the effectiveness of flu vaccines in preventing influenza and complications in healthy adults and included a clear warning:

“Influenza vaccines have a modest effect in reducing influenza symptoms and working days lost. There is no evidence that they affect complications, such as pneumonia, or transmission.

WARNING: This review includes 15 out of 36 trials funded by industry (four had no funding declaration). An earlier systematic review of 274 influenza vaccine studies published up to 2007 found industry funded studies were published in more prestigious journals and cited more than other studies independently from methodological quality and size.

Studies funded from public sources were significantly less likely to report conclusions favorable to the vaccines. The review showed that reliable evidence on influenza vaccines is thin but there is evidence of widespread manipulation of conclusions and spurious notoriety of the studies. The content and conclusions of this review should be interpreted in light of this finding.”

Does Vitamin D Outperform Flu Vaccine?

According to reporter Sun of The Washington Post, I lie when I say that maintaining adequate vitamin D levels outperforms the flu vaccine, yet published studies have come to this exact conclusion and the results have been published by other mainstream reporters.

For example, in 2017, BBC News reported27 the findings of a systematic review28 published in The BMJ, which concluded that vitamin D supplementation protected against acute respiratory tract infection.

The number needed to treat (NNT) was 33, meaning 33 people had to take the supplement in order to prevent a single case of infection. Among those with severe vitamin D deficiency at baseline, the NNT was 4.

As reported by BBC News,29 “That is more effective than flu vaccination, which needs to treat 40 to prevent one case,30 although flu is far more serious than the common cold.”

The BBC actually downplays the findings when it says “flu is far more serious than the common cold,” because the NNT of 40 that BBC News cites refers to the overall effectiveness of inactivated vaccine against influenza-like illness (ILI), which the World Health Organization defines31 as “an acute respiratory infection.” (About 80 percent of all lab tested ILI cases do not test positive for A or B influenza but are caused by other types of viral and bacterial infections.)32

In other words, comparing the NNT of 33 for vitamin D with 40 for the flu vaccine is entirely accurate and appropriate as far as ILI or acute respiratory infection is concerned.

According to the Cochrane Database of Systematic Reviews cited by the BBC, to prevent one case of confirmed influenza, the NNT for inactivated vaccines was 71.33 The Harvard Gazette also published the findings of that BMJ study under the headline, “Study Confirms Vitamin D Protects Against Colds and Flu.”34

The Link Between Influenza and Vitamin D

The association between low vitamin D levels and influenza has been recognized for some time (although low vitamin D levels may not be the sole factor responsible for the seasonality increases of influenza and ILI35). As noted in “Epidemic Influenza and Vitamin D,” published in the journal Epidemiology and Infection in 2006:36

“An interventional study showed that vitamin D reduces the incidence of respiratory infections in children. We conclude that vitamin D, or lack of it, may be Hope-Simpson's ‘seasonal stimulus.’”

Similarly, a 2010 study37 in The American Journal of Clinical Nutrition concluded that “vitamin D3 supplementation during the winter may reduce the incidence of influenza A” in schoolchildren, especially those “who had not been taking other vitamin D supplements and who started nursery school after age 3.”

A 2009 systematic review38 of randomized controlled trials in which supplemental vitamin D was assessed for its ability to prevent or treat various infectious diseases found that the strongest evidence supporting the use of vitamin D existed for tuberculosis, influenza and viral upper respiratory tract illnesses.

In 2018, a randomized, controlled clinical trial39 published in The Pediatric Infectious Disease Journal found that infants receiving high doses of vitamin D who went on to develop influenza had significantly shorter duration of illness compared to those who received a lower dosage.

According to the authors, “High-dose vitamin D (1200 IU) is suitable for the prevention of seasonal influenza as evidenced by rapid relief from symptoms, rapid decrease in viral loads and disease recovery.”

A shortcoming of many (if not most) studies looking at vitamin D’s effects on preventing ILI and/or influenza is that they focus on dosage rather than blood levels, and we now know that it’s achieving a certain blood level that matters, not how much vitamin D it takes to get there. Most studies also use dosages around 1,000 or 2,000 IU’s a day, which are unlikely to raise blood levels of vitamin D to any significant degree.


House Resolution 344 Printer's Number 3193   

A Resolution urging pharmaceutical companies, manufacturers and distributors of prescription opioid drugs to fully cooperate with the Pennsylvania Office of Attorney General in reaching financial settlements and legal resolutions that reflect the severe, irreversible harm suffered by tens of thousands of Pennsylvania families who have lost loved ones to the opioid crisis and to substance use disorder. - Human Services, January 22, 2020

Treatment-resistant and multi-therapy-resistant criteria for bipolar depression: consensus definition.   

Related Articles

Treatment-resistant and multi-therapy-resistant criteria for bipolar depression: consensus definition.

Br J Psychiatry. 2019 01;214(1):27-35

Authors: Hidalgo-Mazzei D, Berk M, Cipriani A, Cleare AJ, Florio AD, Dietch D, Geddes JR, Goodwin GM, Grunze H, Hayes JF, Jones I, Kasper S, Macritchie K, McAllister-Williams RH, Morriss R, Nayrouz S, Pappa S, Soares JC, Smith DJ, Suppes T, Talbot P, Vieta E, Watson S, Yatham LN, Young AH, Stokes PRA

BACKGROUND: Most people with bipolar disorder spend a significant percentage of their lifetime experiencing either subsyndromal depressive symptoms or major depressive episodes, which contribute greatly to the high levels of disability and mortality associated with the disorder. Despite the importance of bipolar depression, there are only a small number of recognised treatment options available. Consecutive treatment failures can quickly exhaust these options leading to treatment-resistant bipolar depression (TRBD). Remarkably few studies have evaluated TRBD and those available lack a comprehensive definition of multi-therapy-resistant bipolar depression (MTRBD).AimsTo reach consensus regarding threshold definitions criteria for TRBD and MTRBD.
METHOD: Based on the evidence of standard treatments available in the latest bipolar disorder treatment guidelines, TRBD and MTRBD criteria were agreed by a representative panel of bipolar disorder experts using a modified Delphi method.
RESULTS: TRBD criteria in bipolar depression was defined as failure to reach sustained symptomatic remission for 8 consecutive weeks after two different treatment trials, at adequate therapeutic doses, with at least two recommended monotherapy treatments or at least one monotherapy treatment and another combination treatment. MTRBD included the same initial definition as TRBD, with the addition of failure of at least one trial with an antidepressant, a psychological treatment and a course of electroconvulsive therapy.
CONCLUSIONS: The proposed TRBD and MTRBD criteria may provide an important signpost to help clinicians, researchers and stakeholders in judging how and when to consider new non-standard treatments. However, some challenging diagnostic and therapeutic issues were identified in the consensus process that need further evaluation and research.Declaration of interestIn the past 3 years, M.B. has received grant/research support from the NIH, Cooperative Research Centre, Simons Autism Foundation, Cancer Council of Victoria, Stanley Medical Research Foundation, MBF, NHMRC, Beyond Blue, Rotary Health, Geelong Medical Research Foundation, Bristol Myers Squibb, Eli Lilly, Glaxo SmithKline, Meat and Livestock Board, Organon, Novartis, Mayne Pharma, Servier, Woolworths, Avant and the Harry Windsor Foundation, has been a speaker for Astra Zeneca, Bristol Myers Squibb, Eli Lilly, Glaxo SmithKline, Janssen Cilag, Lundbeck, Merck, Pfizer, Sanofi Synthelabo, Servier, Solvay and Wyeth and served as a consultant to Allergan, Astra Zeneca, Bioadvantex, Bionomics, Collaborative Medicinal Development, Eli Lilly, Grunbiotics, Glaxo SmithKline, Janssen Cilag, LivaNova, Lundbeck, Merck, Mylan, Otsuka, Pfizer and Servier. A.C. has received fees for lecturing from pharmaceutical companies namely Lundbeck and Sunovion. A.J.C. has in the past 3 years received honoraria for speaking from Astra Zeneca and Lundbeck, honoraria for consulting from Allergan, Janssen, Lundbeck and LivaNova and research grant support from Lundbeck. G.M.G. holds shares in P1Vital and has served as consultant, advisor or CME speaker for Allergan, Angelini, Compass pathways, MSD, Lundbeck, Otsuka, Takeda, Medscape, Minervra, P1Vital, Pfizer, Servier, Shire and Sun Pharma. J.G. has received research funding from National Institute for Health Research, Medical Research Council, Stanley Medical Research Institute and Wellcome. H.G. received grants/research support, consulting fees or honoraria from Gedeon Richter, Genericon, Janssen Cilag, Lundbeck, Otsuka, Pfizer and Servier. R.H.M.-W. has received support for research, expenses to attend conferences and fees for lecturing and consultancy work (including attending advisory boards) from various pharmaceutical companies including Astra Zeneca, Cyberonics, Eli Lilly, Janssen, Liva Nova, Lundbeck, MyTomorrows, Otsuka, Pfizer, Roche, Servier, SPIMACO and Sunovion. R.M. has received research support from Big White Wall, Electromedical Products, Johnson and Johnson, Magstim and P1Vital. S.N. received honoraria from Lundbeck, Jensen and Otsuka. J.C.S. has received funds for research from Alkermes, Pfizer, Allergan, J&amp;J, BMS and been a speaker or consultant for Astellas, Abbott, Sunovion, Sanofi. S.W has, within the past 3 years, attended advisory boards for Sunovion and LivaNova and has undertaken paid lectures for Lundbeck. D.J.S. has received honoraria from Lundbeck. T.S. has reported grants from Pathway Genomics, Stanley Medical Research Institute and Palo Alto Health Sciences; consulting fees from Sunovion Pharamaceuticals Inc.; honoraria from Medscape Education, Global Medical Education and CMEology; and royalties from Jones and Bartlett, UpToDate and Hogrefe Publishing. S.P. has served as a consultant or speaker for Janssen, and Sunovion. P.T. has received consultancy fees as an advisory board member from the following companies: Galen Limited, Sunovion Pharmaceuticals Europe Ltd, myTomorrows and LivaNova. E.V. received grants/ research support, consulting fees or honoraria from Abbott, AB-Biotics, Allergan, Angelini, Dainippon Sumitomo, Ferrer, Gedeon Richter, Janssen, Lundbeck, Otsuka and Sunovion. L.N.Y. has received grants/research support, consulting fees or honoraria from Allergan, Alkermes, Dainippon Sumitomo, Janssen, Lundbeck, Otsuka, Sanofi, Servier, Sunovion, Teva and Valeant. A.H.Y. has undertaken paid lectures and advisory boards for all major pharmaceutical companies with drugs used in affective and related disorders and LivaNova. He has also previously received funding for investigator-initiated studies from AstraZeneca, Eli Lilly, Lundbeck and Wyeth. P.R.A.S. has received research funding support from Corcept Therapeutics Inc. Corcept Therapeutics Inc fully funded attendance at their internal conference in California USA and all related expenses. He has received grant funding from the Medical Research Council UK for a collaborative study with Janssen Research and Development LLC. Janssen Research and Development LLC are providing non-financial contributions to support this study. P.R.A.S. has received a presentation fee from Indivior and an advisory board fee from LivaNova.

PMID: 30520709 [PubMed - indexed for MEDLINE]


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Op-ed | What should we call the men and women of Space Force?   

Space News: Last year, I was invited by the U.S. government to a couple of workshops to help visualize future scenarios and strategies, which triggered a question in my mind: So what do you call members of the Space Force in all their varied roles? Several things must be considered: There is no centuries-old tradition to inform our choice. The traditions that do exist in other services can be inconsistent and confusing. Science fiction and culture have already set some expectations, both good and bad (starship trooper, space cadet, spaceman spiff). We have a preexisting space culture with its own terminology, namely “astronaut” for those who actually fly in space. The new service is being carved from the Air Force, but space is seen as analogous to the sea and thus the domain of the sea services and nautical terminology enter the discussion. Any term should be usable as a formal designation for lower ranks. It should cover all members of the service. Everyone in the Navy, from ensign to admiral, is a Sailor. In the Army, all are Soldiers. In the Marine Corps, it’s Marine. And in the Air Force, all service members are Airmen (male or female — an awkward ...



VAT, NBT tax cuts for school uniforms: Siyambalapitiya

The government is planning to add the benefit of Value-added Tax (VAT) and Nation-building Tax (NBT) tax cuts to school uniform vouchers, Education Minister Ranjith Siyambalapitiya said. He made this observation in Parliament, yesterday, while denying allegations that the value of the school uniform vouchers was lessened.

“The VAT and nation-building taxes are included in the value of the vouchers. Following the tax cuts, we believe that the benefit should go to the students.” Minister Siyambalapitiya said.

He added that the government is to swiftly look into the difficulties faced by the teachers and students at the Polonnaruwa National College of Education. People's Liberation Front MP Bimal Rathnayake, during the oral question round, informed the Education Minister that there is a serious lack of facilities at the Polonnaruwa National College of Education. “Apparently, there is a serious water shortage in the college, and sanitary facilities are not in operation either. I would like the Education Minister to quickly look into this matter,” MP Rathnayake said.

In reply, Minister Siyambalapitiya said he would quickly address any issues at the training college.

Following a question raised by United National Party MP Hesha Withana, Minister Siyambalapitiya assured that the government is planning to carry out the recruitment process of teaching assistants to government schools in a transparent manner.

The minister said the recruitment process would most probably include a competitive examination, as usual.

“We are yet to finalise how the process would take place, and I assure that it will be a transparent one,” he said.


‘Agriculture Ministry to return to Govijana Mandiraya by month’s end’

Agriculture Minister Chamal Rajapaksa affirmed that the Agriculture Ministry would be shifted by the end of the month from the DPJ building in Rajagiriya to its original building, the Govijana Mandiraya.

He said negotiations are under way with the owners of this building, and that legal provisions are being looked at to see if the owners of the building could be persuaded to end the lease and release the Agriculture Ministry from the agreement, which is due to lapse in March 2021.

Addressing a media briefing in Parliament, yesterday, the minister said that despite the agreement signed by the previous government to obtain this building for a colossal rent of Rs.24.4 million per month, and having obtained Cabinet approval for it, this building lacks adequate parking space—and most of the vehicles have to be parked on the narrow side road nearby, or on the main road. He also noted that despite this high rent, all the partitioning and furnishing had been done on the government’s expense.

The previous government is said to have paid off the lease for the building in Rajagiriya, which has so far housed the Agriculture Ministry, until the end of the term in March 2021, it is reported. According to the agreement, even if the tenants vacate the building prior to the end of the 5-year lease term, the owner would not return the money paid for the entire period.

He said that in the event the owners of the building does not agree to terminate the lease agreement, the Agriculture Ministry would still vacate the building and move to the Govijana Mandiraya; but another state institution occupying private premises where their lease agreement is about to expire, would be relocated to at the DPJ building until the lease term ends in 2021. Minister Rajapaksa said that by housing all 25 divisions under the Agriculture Ministry under one roof at the Govijana Mandiraya in Battaramulla, it would make it easier for farmers to get all required services under one roof, without having to waste their time unnecessarily.


Speaker asks for names of COPE, COPA nominees

Speaker Karu Jayasuriya, at the Selection Committee meeting held in Parliament, yesterday, requested the government and the Opposition to provide the names of the nominees for committees such as COPE and COPA without delay.

The Selection Committee decided to constitute the Committee of Parliamentary Business on January 23. The Speaker is to table the names of the MPs who will represent the Committee on Parliamentary Business.

The Selection Committee also decided to appoint the Committee on High Posts, today.

Parliamentarians Dinesh Gunawardena, Johnston Fernando, Mahinda Samarasinghe, Sajith Premadasa, John Amaratunga, Mano Ganesan, and Niroshan Perera were also present at the meeting.


Rs.21,708 mn Supplementary Allocation presented to Parliament

A Supplementary Allocation of Rs.21,708 million was presented to Parliament, yesterday, seeking House approval for the expenses incurred from November 1 to 30, provisioning 73 different programmes and purposes.

In order to meet the additional allocation provided to meet the increased cost of fuel, vehicles, plant and machinery maintenance, postal and communication, and electricity and water supply for the President, the government has also sought House approval for an additional allocation of Rs.330 million using the Supplementary Allocation.

The Ministry of Agriculture, Rural Economic Affairs, Livestock Development, Irrigation, and Fisheries & Aquatic Resources Development has been allocated an additional sum of Rs.350 million for the capital expenses of the Agriculture Sector Modernisation Project, and an additional Rs.240 million for the expenses on Climate Smart Irrigated Agriculture Project.

Rs.2.4 billion was allocated to the Treasury to meet the shortfall of provisions for interest payments on bank overdraft and other debt, followed by Rs.2 billion to the Department of Pensions to shoulder the revision of pensions.

The Sri Lanka Railways Department has been allocated Rs.450 million to pay Customs Import Duty, Nation Building Tax, Value Added Tax for purchasing three sets of diesel electrical locomotives.

Rs.3.1 billion has been allocated to the Ministry of Health, Nutrition and Indigenous Medicine to settle the bills relating to medical supplies to State Pharmaceutical Corporation and State Pharmaceutical Manufacturing Corporation.

The Ministry of Megapolis and Western Development has been allocated Rs.4.5 billion to implement town development in nine provinces, restoration of water quality in the Beira Lake, restoration of the Jaffna Town Hall, the Sahasra Bus Programme, the Metro Colombo Solid Waste Management System, and the Urban Regeneration Programme.

Supplementary allocations are being provided in terms of Clause 6 (1) of the Appropriation Act, as required.

These are provided strictly for the purposes specified in approved Budget Estimates to relevant spending agencies, having carried out a needs assessment while giving consideration to the relevant financial regulations and approved procedures.

However, the supplementary provision presented yesterday did not change the approved total expenditure limits of the annual estimate by Parliament.

The allocation of such purposes has been made under the Project of Budgetary Support Services and Contingent Liabilities of the Department of National Budget, and it is under the limit of the Approved Annual Budget.

Therefore, either the borrowing limit or the maximum limit of the total expenditure will not be increased due to the granting of these supplementary provisions.

The purpose of this provision is to facilitate the smooth conduct of public finance management in a more efficient and effective manner.


Ranjan’s telephone conversations: Hemapala gives statement to CCD

Baddegama Magistrate Dhammika Hemapala, who was interdicted as part of ongoing investigations into the alleged telephone conversations he had with Parliamentarian Ranjan Ramanayake, yesterday arrived at the Colombo Crimes Division to give statement. The CCD official has recorded a statement in connection with the telephone conversation from him for over two hours. Hemapala left the CCD premises around 5.15 p.m.

Wednesday, January 22, 2020 - 01:00


Product Specialist - Immunology - KSA National   

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LocationSaudi ArabiaJob TypeDirectHoursFull TimeRequired Years of Experience5Required EducationBachelors DegreeJob DescriptionA reputable and well established multinational pharmaceutical company is actively recruiting for a Human Resource Business Partner (SAUDI NATIONAL) to be based in Riyadh KSA This client has the ability and reputatio

Search And Rescue Addendum To The National Search And Rescue Supplement To The International Aeronautical And Maritime Search And Rescue Manual Version 10   

Search And Rescue Addendum To The National Search And Rescue Supplement To The International Aeronautical And Maritime Search And Rescue Manual Version 10

Haybury: Global Medical Lead -Rare Disease/Genetic Disorders   

Excellent: Haybury: A fantastic opportunity has arisen for a Global Medical Lead to join one of the top 20 pharmaceutical companies in the world. This exciting role ba... United States

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Продам новую женскую куртку бренда nautica р.40   

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2020-81066 - Manufacturing Engineer 3   

Main domain/Job field : Production/Industrial Engineering
Employment type : Permanent
Position description :
Job Summary: Supports the engineering and production departments with respect to the manufacturing of aircraft interior products by solving manufacturing issues and reducing the time to manufacture products with the implementation of time saving measures. The Manufacturing Engineer will ensure the quality, integrity and certification properties of products manufactured is maintained or improved. Summary of Duties: • Act as shop liaison between design engineers and production to ensure products are built to specifications and engineering documents. • Provide feedback to design engineering to improve product design for ease of manufacturing, optimization of cost, weight reduction and time to manufacture product. • Prepare engineering change requests (CRs) as required to support manufacturing and quality of parts produced. • Identify and, if necessary, design and deploy tooling to aid in production processes. • Ensure standardization and compliance to engineering, customer and company specification for processes employed in the production of interior products. • Solve manufacturing issues and communicate solutions to design engineering. • Establish manufacturing line set up for new products for optimal production with respect to time and cost. • Provide assistance to production personal for all facets related to manufacturing of product. • Know and apply C&D engineering manual, CDE1000 with emphasis on Section 2.0. • Identify and deploy improvements on the shop floor • Review 2D drawings for manufacturability • Analyze process and product risks

Level 3 Qualifications: Education: BS in Industrial, Aeronautical, Mechanical Engineering or Manufacturing Engineering Experience: 6+ years. Computer Skills: Proficient with Windows Operating System®, Office XP®., AutoCAD. Knowledge of design software Other Skills: Experience with airworthiness regulations, and LEAN tools such as Valve Stream Mapping (VSM) “5S”. Advanced knowledge of pull systems standardized work and strong problem solving skills. Description: Senior-level position within job role.
City (-ies) : Cypress
Minimum education level achieved : Bachelor's Degree




The 1990's are alive and well!!! Barenaked Ladies have just rolled out the band's sixth "Last Summer On Earth Tour" -- with the 2020 edition featuring special guests the Gin Blossoms and Toad The Wet Sprocket. The bands kick off the 34-city jaunt on June 3rd at St. Augustine, Florida's Saint Augustine Amphitheatre and wrap things up seven weeks later on July 23rd Toronto's Budweiser Stage.

Barenaked Ladies frontman Ed Robertson told us the mindset of the band when it comes to touring has changed over the years because they now see performing as their job, which they need to work hard at: "We're trying to practice sustainable development within the band. I think the way a lot of us used to exist was to throw ourselves into the band and try and live our lives in the time off. And recently, I think what we've been trying to do is recognize the fact that we're in this band and we've got to work really hard and we have to live our lives while we do it."

Gon Blossoms guitarist Jesse Valenzuela explained that aside from the band members' move into middle age, little has changed for them when it comes to hitting the road: "Y'know what, it hasn't changed that much. There's a total lack of enthusiasm right before the show, and then someone says, 'Let's get this thing over with,' and then they go out and play really hard, as hard as they can. I don't know why, it's like they're saving their energy. And then after the show there's this horrible post-mortem and then there's this low-grade bickering, and then we go back to the hotel and then the guys adjourn to somebody's room and have a little party."

JUST ANNOUNCED: Barenaked Ladies / Gin Blossoms / Toad The Wet Sprocket tour dates (subject to change):

June 3 - St. Augustine, FL - Saint Augustine Amphitheatre
June 4 - Atlanta, GA - Cadence Bank Amphitheatre
June 6 - Houston, TX - Revention Music Center
June 7 - Irving, TX - The Pavilion at Toyota Music Factory
June 11 - Phoenix, AZ - Arizona Federal Theatre
June 12 - Los Angeles, CA - Greek Theatre
June 13 - San Diego, CA - Cal Coast Credit Union Open Air Theatre
June 14 - Paso Robles, CA - Vina Robles Amphitheatre
June 16 - Saratoga, CA - The Mountain Winery
June 18 - Redmond, WA - Marymoor Amphitheater
June 19 - Troutdale, OR - Edgefield
June 20 - Airway Heights, WA - Northern Quest Resort & Casino
June 23 - Morrison, CO - Red Rocks Amphitheatre
June 25 - Kansas City, MO - Starlight Theatre
June 26 - Prior Lake, MN - Mystic Lake Casino
June 27 - Council Bluffs, IA - Stir Concert Cove at Harrah's Council Bluffs
June 29 - Chicago, IL - Chicago Theatre
July 1 - St. Louis, MO - TBA
July 3 - Cleveland, OH - Jacobs Pavilion at Nautica
July 4 - Clarkston, MI - DTE Energy Music Theatre
July 5 - Indianapolis, IN - White River State Park
July 7 - Lewiston, NY - Artpark Amphitheater
July 8 - New York, NY - Central Park SummerStage
July 10 - Gilford, NH - Bank of New Hampshire Pavilion
July 11 - Uncasville, CT - Mohegan Sun Arena
July 12 - Boston, MA - Rockland Trust Bank Pavilion
July 14 - Philadelphia, PA - The Met
July 15 - Vienna, VA - Wolf Trap
July 17 - Charleston, SC - Volvo Car Stadium
July 18 - Raleigh, NC - Red Hat Amphitheater
July 19 - Baltimore, MD - MECU Pavilion
July 21 - Cincinnati, OH - PNC Pavilion at Riverbend
July 22 - Pittsburgh, PA - Stage AE
July 23 - Toronto, ONT - Budweiser Stage




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Ghana: 3 Merged Pharmaceutical Companies List On Accra Bourse   

[Ghanaian Times] Dannex Ayrton Starwin (DAS) Plc has been listed on the Ghana Stock Exchange (GSE) to give opportunity to both local and foreign investors to invest in the company.

Make code on pharma firms mandatory: doctors   

Make code on pharma firms mandatory: doctors
The Alliance of Doctors for Ethical Healthcare has demanded that the Uniform Code of Pharmaceutical Marketing Practices be made mandatory. “It is unfo

Source: TH



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CHOFER - Pisa Farmacéutica - Mérida, Yuc.   

Reparto de mercancía o mensajería. En grupo PISA somos más de 18,000 Profesionales comprometidos a contribuir con la preservación del bien más valioso de todos,…
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Professions: Clinical Site Monitoring Manager - Olathe, Kansas   

Job is remote but Candidate must reside in Kansas, Nebraska, or Missouri Clinical Site Monitoring Manager needs 5 years monitoring experience in a pharmaceutical or medical device company or clinical research organization Clinical Site Monitoring Manager requires: Experience working in more than one therapeutic area Allied Health Professions degree (PA, RN, RPh), relevant clinical experience or four-year life science degree Familiar with Electronic Data Capture preferred Experience with Risk Based Monitoring preferred Strong knowledge, understanding, and application of monitoring SOPs and Good Clinical Practice Good working knowledge of the drug development process Advanced skills in Microsoft Word, Microsoft PowerPoint, Microsoft Excel, Microsoft Outlook, Global Site Management Operations Subject Matter Expert (SME) Clinical Site Monitoring Manager duties: Must work effectively and efficiently in a home-based office environment Will maintain a fully functional home office (high speed internet connection, office phone, copier, etc.) May potentially travel overnight an average of 50% May be required to lift more than 25 pounds, in association with travel requirements. Must maintain a credit limit that would support routine business travel expenses. Manage all site activities Communicate site status and monitoring activities Meet all departmental timelines and deliverables Attend and participate in all relevant meetings Lead Site Manager Global Site Management Operations Subject Matter Expert (SME) Oversight Representative ()

Mechanic, Production Maintenance - Taro Pharmaceuticals Inc. - Brampton, ON   

Mechanical, electrical, hydraulic, instrumentation prints. Science-based pharmaceutical company dedicated to meeting the needs of its customers through the…
From Taro Pharmaceuticals Inc. - Tue, 21 Jan 2020 00:38:53 GMT - View all Brampton, ON jobs

Criação do Ministério da Aeronáutica completa 79 anos   

Para celebrar a data, INCAER realiza até o próximo dia 21 uma exposição sobre Santos-Dumont e a Força Aérea Brasileira

FAB lança vídeo em homenagem ao Dia de criação do Ministério da Aeronáutica   

Data é celebrada dia 20 de janeiro

Other: QA/QC Inspector - Malta - Albany, New York   

QA/QC INSPECTOR - MALTA Exyte is a global leader in the design, engineering and delivery of facilities for high-tech industries. With a history of more than 100 years, the company has developed a unique expertise in controlled and regulated environments. Exyte has a truly global footprint, serving the most technically demanding clients in markets such as semiconductors, batteries, pharmaceuticals, biotechnology, and data centers. The company offers a full range of services from consulting to the managing of turnkey solutions delivered to the highest quality and safety standards. Solving the most complex challenges, Exyte forges trusted, long-lasting relationships with its clients. In 2018, Exyte generated sales of EUR 3.5 billion with over 5,600 highly experienced and motivated employees. The company is ideally positioned to further strengthen its market leadership with its broad industry insight and its exceptional talents. *Performs material inspection *Performs weld inspection *Performs installation inspections *Conformance / non-conformance reporting *Performs hydrostatic pressure test *Performs pneumatic pressure test *Performs inboard helium leak detection *Performs outboard helium leak detection *Performs particle sampling analysis *Performs trace moisture and oxygen analysis *Documents and archives per published TFS procedures *Performs Borescope video inspections *Creates Safety Observation Reports *Other duties as assigned *High School Diploma or GED required *Certified Welding Inspector required *American Society for Non-destructive Testing (ASNT) Level II preferred *3+ years of experience Attractive salaries, supportive environments and excellent benefits allow for growth and career development with Exyte Group. NO OUTSIDE RECRUITERS OR AGENCIES Exyte Group is an Equal Employment Opportunity Employer. The Exyte Group provides equal employment opportunities to all qualified applicants without regard to race, sex, sexual orientation, gender identity, national origin, color, age, religion, protected veteran or disability status, or genetic information. Nearest Major Market: Albany Job Segment: Inspection, Engineer, Welding Inspector, Welding, Consulting, Engineering, Manufacturing, Technology ()

Wrongful-Death Lawsuits Filed By Prince’s Family Dismissed   


A series of wrongful death lawsuits filed by Prince’s family members have been dismissed, TheWrap has learned.

The Associated Press first reported the news, saying it’s almost certain that Prince’s family members reached a settlement with the defendants in the cases, including Walgreens, an Illinois hospital and a Minnesota doctor who all treated him in the weeks before he died. However, details have not been disclosed.

Attorneys on the case either did not return a request for comment or declined to comment as to the nature of a settlement.

John Goetz, an attorney representing Prince’s estate, clarified that one medical negligence claim against Howard Kornfeld still remains alive on appeal. Kornfeld is a California addiction specialist who was contacted by Prince’s associates before his death.

The artist’s family said Kornfeld had a duty to advise his associates that Prince should be recommended for treatment, but the judge found no evidence that Kornfeld had ever communicated with Prince or that a relationship was established. The case was dismissed in September, but the plaintiffs have appealed.

Prince’s family filed wrongful-death lawsuits beginning in April 2018, but some of the claims were quietly dismissed as early as last summer.

In August, claims against the pharmaceutical chain Walgreens and the Trinity Medical Center in Illinois were dismissed, and in November, claims against Dr. Michael Schulenberg and his former employer were both permanently dismissed in November 2019. Schulenberg and the Trinity Medical Center treated Prince in the weeks before his death, and Walgreens filled his prescriptions.

Prince died at age 57 on April 21, 2016 of an accidental fentanyl overdose. No criminal charges were filed related to his death, and the source of the counterfeit pills that killed him remains unknown.

Prince died without a will, and his estate was once valued at around $200 million.

Pamela Chelin contributed to this report.

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CNN Settles Defamation Lawsuit With Covington Student Nicholas Sandmann

Lawsuit That Accused Miley Cyrus of Copyright Infringement Is Settled


Comandante da Força Aérea, Brigadeiro Bermudez se pronuncia sobre Venezuela e Operação Acolhida - Gov. Bolsonaro   


Em pronunciamento por ocasião de cerimônia alusiva à Operação Acolhida, a qual ocorre na fronteira com a Venezuela e é gerida pelo Exército Brasileiro com a finalidade de acolher imigrantes do país vizinho, o Tenente-Brigadeiro Bermudez, Comandante da Aeronáutica, representou o Ministro da Defesa, General Fernando Azevedo.
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A Focus on Excellence

Understanding the critical importance of eye health, our optical team members provide patients with outstanding services and care.


Optometrist – Part-Time (20 hrs/wk)

Elk Grove, California


In this role, you will perform routine procedures using independent professional judgment in the practice of optometry within the scope of the laws of the state of California, the rules and regulations of the California Board of Optometry, and the policies of The Permanente Medical Group, Inc..


Qualifications Include:

At least one year of experience preferred
OD degree from an accredited School of Optometry
A current California Optometric License
Therapeutic Pharmaceutical Agents (TPA.) required for external employees hired after November 2009 (TPA is not required for internal applicants)
A National Provider Identifier (NPI) or the ability to obtain one prior to employment start date
The ability to meet all the specifications of staff Optometrist
The ability to work in a Labor Management Partnership environment


For immediate consideration, please visit  or for complete qualifications and job submission details, referencing job number 847967 or 847975.


Kaiser Permanente is an equal opportunity employer committed to a diverse and inclusive workforce. Applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy), age, sexual orientation, national origin, marital status, parental status, ancestry, disability, gender identity, veteran status, genetic information, other distinguishing characteristics of diversity and inclusion, or any other protected status.


External hires must pass a background check/drug screen. Qualified applicants with arrest and/or conviction records will be considered for employment in a manner consistent with federal and state laws, as well as applicable local ordinances, including but not limited to the San Francisco and Los Angeles Fair Chance Ordinances.


This position supports Kaiser Permanente’s code of conduct and compliance by adhering to all laws and regulations, accreditation and licensure requirements, and internal policies and procedures.




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Sun Pharma Outlook for the Week (Jan 20, 2020 – Jan 24, 2020)   

EquityPandit’s Outlook for Sun Pharma for the week (Jan 20, 2020 – Jan 24, 2020): SUN PHARMA: BSE: 524715| NSE: SUNPHARMA| ISIN: INE044A01036 | SECTOR: PHARMA Stock closed the week on positive note gaining +2.43% Week High: 458.25 Week Low: 444.50 Week Range: 13.75 Points Sun Pharmaceutical Industries Ltd. Technically on the daily charts EquityPandit’s Analyst […]

Zimbabwe: ZACC Probes Drug Thefts At Hospitals   

[The Herald] The Zimbabwe Anti-Corruption Commission (ZACC) is now monitoring public hospitals and clinics to curb thefts and ensure drugs are not diverted to the black market. This follows checks that were done at the country's drug procurement and supply entity, the National Pharmaceutical Company (Natpharm).

Rwanda: Diabetes Patients to Get Free Self-Testing Devices   

[New Times] Type 1 Diabetes patients in the country will soon have free self-testing devices, for four years, thanks to a partnership between the Ministry of Health and Abbot, an American pharmaceutical company.

Data Center -IT Project Manager   

NJ-Princeton, Title: Data Canter Project Manager Location:Princeton (Nassau Park), NJ Duration: 6 to 11 Months Looking for the below experience & skills IT, Data Center, PM, Facilities, DC Relocations, Pharmaceuticals Thank you, Chris Wilson Team Recruitment Desk#: 678-496-7811 ABOUT ACS GROUP. - ACS Group is a premier provider of IT Consulting, Engineering Consulting, Healthcare, Talent, and Workforce Manageme

Business Analyst IT - II (Experienced) (remote possibility)   

NJ-Branchburg, Req#: 27374 Title: IT Business Analyst II Location: Branchburg, NJ 08876 (Remote Flexibility) Duration: 12+ Month Contract Target Comp: $50/hr. One of the nation's top Pharmaceutical organizations consistently ranked as one of the “Great Places to Work” in the country, is seeking a confident and experienced IT Business Analyst who has a strong SAP and Financial background. Qualifications: Min. of

Reinsurer Appeals Judgment, Adverse Orders In Dispute With Insurer Over Billings   

UTICA, N.Y. - A reinsurer on Dec. 27 told a New York federal court that it is appealing a $6.25 million judgment in favor of an insurer and prior adverse orders in a dispute between the parties over coverage under two separate reinsurance certificates for settlements of asbestos claims (Utica Mutual Insurance Co. v. Century Indemnity Co., No. 13-995, N.D. N.Y.).
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