What is role of qualified person for pharmacovigilance

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What is the role of a Qualified Person for Pharmacovigilance (QPPV) and what are they responsible for managing/overseeing as part of a robust pharmacovigilance system? In light of Brexit what aspects, if any, need to be considered with regard to the Qualified Person for Pharmacovigilance (QPPV) relationship between the UK and remainder of the EU?

Reference no: EM133274310

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