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The company was correct, as a federal judge struck down the verdict last week for being inconsistent. Fresenius oncology drug plant slammed with new warning letter. A Fresenius Kabi cancer drug plant in India savaged by the FDA in the past for hiding serious drug testing issues, has been branded with a new warning letter.
Mallinckrodt, which has landed in hot water multiple times this year, is diversifying beyond its controversial lead seller. Roche snags another Perjeta combo nod, but will 'weak' data limit its use? Roche landed an end-of-the-year indication for Perjeta, but it's an indication analysts and investors think may not be as lucrative as they once hoped.
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Try exercise to improve memory, thinking. For patients with mild cognitive impairment, don't be surprised if your health care provider prescribes exercise rather than medication. A new guideline for medical practitioners says they should recommend twice-weekly exercise to people with mild cognitive impairment to improve memory and thinking. Zika remains a research and public health challenge.
Sincewhen Zika was declared by the World Health Organization as a public health emergency of international concern, the virus has become established in more than 80 countries, infected millions of people, and left many babies with birth defects collectively called congenital Zika syndrome. Although scientists have made progress [ AZ and ICL link to research respiratory diseases. AstraZeneca and Imperial College London have announced plans to work together on investigating the scientific mechanisms and underlying drivers of respiratory conditions such as asthma and chronic obstructive pulmonary disease COPD.
FDA updates the label of Tasigna to reflect that certain patients with a type of leukemia may be eligible to stop treatment after sustained response.
Roche and Ignyta reach definitive merger agreement.
Cost regulators for NHS treatments in England and Wales have turned down Roche's Tecentriq for patients who have already received prior treatment for metastatic urothelial cancer.
The FDA published guidance assisting sponsors in evaluating the effects of psychoactive drugs on the ability to operate a motor vehicle. Data obtained early in development can be used to guide the [ The European Medicines Agency adopted a guideline for sponsors developing new products for autism spectrum disorder, providing recommendations on diagnostic criteria, target populations and clinical trial design.
The European Medicines Agency adopted the fifth revision of its substantive guideline covering all stages of oncology drug development, expanding upon the previous version's section on Atlantis Casino Com data.
The European Medicines Agency and the European Network for Health Technology Assessment released a joint work plan to help medicine developers improve clinical research and become more efficient in generating the evidence needed for both agencies.
Protocol September 03, About CSG Clinical Safety Geek was founded in with the sole purpose of creating a helpful tool and resource for clinical development with special emphasis on the oncology disease area.
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