Pharmacovigilance is the science and activities relating to the detection, assessment, understanding and prevention of adverse effects or any other medicine-related problem.
The European Medicines Agency (EMA) coordinates the European Union (EU) pharmacovigilance system and operates services and processes to support pharmacovigilance in the EU. It is essential that the safety of all medicines is monitored throughout their use in healthcare practice. EU law requires each marketing authorisation holder, national competent authority and EMA to operate a pharmacovigilance system. The situation is similar in Switzerland, which is not in the EU but has equally strict requirements policed by its agency, SwissMedic. We know and worked with the right consultants whom have extensive experience in pharmacovigilance.
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