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European Medicines Evaluation Agency (EMEA)

2009
Registration authority within the EC and coordinating centre for the centralised procedure, renamed to European Medicines Agency, sited in London; → see also expert detache.
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The European Medicines Agency is still too close to industry:

BMJ, 2016
Two decades after its inception, the agency still fails to put patients’ interests first Fifteen years ago I raised criticisms about the policy and attribution of the then young European Medicines Agency (EMA) and its Committee for Medicinal Products for Human Use (CHMP).1 With the same aim of encouraging this institution to put the interests of ...
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European Medicines Evaluation Agency and the new licensing arrangements

Drug and Therapeutics Bulletin, 1994
Since September 1971 the Medicines Act has provided the legal basis for controlling the manufacture, sale, supply and marketing of medicines in the UK.1 The law has been modified by Parliament and the incorporation of European directives, but until now its interpretation and implementation have remained matters for UK authorities.
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Medicines transparency at the European Medicines Agency (EMA) in the new information age: the perspectives of patients

Journal of Risk Research, 2016
Ragnar Löfstedt   +2 more
exaly  

The European Medicines Agency's strategies to meet the challenges of Alzheimer disease

Nature Reviews Drug Discovery, 2015
Luca Pani   +2 more
exaly  

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