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EMA to provide access to all documents

November 20, 2010 1:27 AM UTC

The European Medicines Agency plans to release an updated policy next week that will make all agency documents available upon request, including clinical trials data and adverse event reports. Under the new policy, anyone will be able to submit a request to EMA, which said it aims to provide the requested information within 15 working days. Larger requests may take longer and involve an administration fee. The agency did say that commercially or personally sensitive information may be redacted. ...