An Essential Overview of Pharmacovigilance
Pharmacovigilance has undergone rapid regulatory change in recent years and become one of the most demanding aspects of the pharmaceutical industry to both understand and comply with. There are many requirements and duties for companies to perform regarding the safety of their products to satisfy regulatory demands, and sanctions for non-compliance can be severe.
EU pharmacovigilance legislation requires companies to train all staff, including those not working directly in pharmacovigilance, and this invaluable one-day course will help you meet that requirement with a concise overview of the pharmacovigilance function and current regulatory requirements.
Benefits of attending:
- Gain an overview of EU pharmacovigilance
- Understand the documentation required by regulatory authorities
- Clarify the roles and responsibilities of a licence holder
- Understand the role of the Qualified Person for Pharmacovigilance (QPPV)
- Review the standard operating procedures (SOPs) in relation to pharmacovigilance
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Reviews by course attendees
Average rating 4.7
It was brill for an overview! Questions were answered by the speaker and the atmosphere made me feel really comfortable and allowed me to ask the questions in a confident way.
Graeme was knowledgeable on all the material. [Overall] very good and informative.
[The speaker was] very professional and knowledgeable.