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Alexander Roussanov

ID:LEX-AR-8A96JFA1

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Organization: Hogan Lovells

The EMA launches a public consultation on eSource Direct Data Capture in clinical trials

Focus on Regulation · November 28, 2018

EMA publishes a Questions & Answers document on the practical implementation of Article 31 Pharmacovigilance Referral procedure

Focus on Regulation · January 29, 2014

The EFPIA and PhRMA principles for responsible sharing of clinical trial data enter into force on 1 January 2014

Focus on Regulation · January 6, 2014

The EMA continues its work towards the implementation of the Policy on the publication and access to clinical trial data

Focus on Regulation · December 19, 2013

Entry in force of the new amendments to the EU pharmacovigilance rules

Focus on Regulation · November 7, 2013

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