EMA advises on transparency requirements of EU clinical trial regulation

Published: 16-Feb-2015
Regulatory

Aims to balance information needs of patients with academia and industry


The European Medicines Agency (EMA) has released a paper explaining its consultation with the pharma industry on proposed transparency reforms to the European Union (EU) clinical trial regulation (Regulation No 536/2014). EMA wants feedback. Its goal is 'to balance carefully the information needs of patients and the public with the needs of academia and industry'.

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