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Author: Dr Tiziana von Bruchhausen
The main success factors for medical writing as a whole also apply to the requirements for writing PV documents. This checklist reduces the error and defect rate enormously. You will also get an insight of the growing requirements for the work of pharmacovigilance.
Download now the white paper 'Medical Writing in Pharmacovigilance'.
5 consecutive webcasts - Pharmacovigilance in China, LATAM, EAEU, MENA, Latin America and on strategic questions
Our global and local experts will update you every two months with the latest regulatory and legislative developments. Thus, you will always have the essential information and trends in regulatory affairs and pharmacovigilance at your fingertips!
During this summer school you will build a solid toxicological know-how basis and will be informed about the inclusion of toxicological data in the marketing authorisation dossier. Take the chance and participate in our interactive online training.
Our global and local experts will update you every two months with the latest regulatory and legislative developments. Thus, you will always have the essential information and trends in regulatory affairs and pharmacovigilance at your fingertips!
