Dr. Mirela Vita

Lead of Clinical Trials Department at the Romanian National Agency for Drugs and Medical Devices, Romania
Dr. Mirela Vita

Graduated Carol Davila University of Medicine and Pharmacy, Faculty of General Medicine

Specialized in Internal medicine and Clinical Pharmacology

Currently Coordinator of Clinical Trial Department of National Agency for Medicine and Medical Devices from Romania and clinical assessor

Working in the NAMMDR for more than 15 years, at the beginning being involved in assessment of medicinal product information and since 2008, in clinical trials assessment and authorization

Member of Clinical Trial Facilitation Group (CTFG) since 2008; clinical trials facilitation group was established in 2004 by the Heads of Medicines Agencies (HMA) to coordinate the implementation of the EU clinical trials directive 2001/20 EC across the member states.

Member of EMA and Member States Group for developing Clinical Trial Information System (the basis of future collaboration between MS in clinical trials assessment according to the new Clinical Trial Regulation)

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