EDPS: Draft clinical trials regulation 'unclear' on data processing
DataGuidance (press release)
On 18 February 2013, the European Parliament will consider a draft report on the clinical trial reforms put forward by Glenis Willmott MEP, the Rapporteur for the Committee on the Environment, Public Health and Food Safety, in charge of the reforms.
Rapporteur Willmott wants tougher transparency in CT Directive revisionPharmaTimes

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