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Pharmacovigilance System Master File – Emerging Requirements
13
Aug
It was July 2012 when the European Medicines Agency made it mandatory for all the marketing authorization holders (MAH) to maintain the Pharmacovigilance System Master File (PSMF) as per the GVP Module II. Until then, the document was a concise one and called as the detailed description of Pharmacovigilance system (DDPS). After the PSMF came […]
Pharmacovigilance in Liechtenstein – Interesting Facts
23
Nov
Liechtenstein is a small country that is located between Austria and Switzerland. Liechtenstein is not a part of the European Union, but it is a part of the European Economic Area (EEA) and the European Free Trade Association (EFTA). Courtesy: Google Maps Switzerland is a part of EFTA, and not a part of EEA. On […]
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