QPPVQualified Person for Pharmacovigilance (drug safety inspector)
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References in periodicals archive ?
It is almost certain that after Brexit, marketing authorization holders (MAHs) will have to put in place a UK-based QPPV, as well as a EU QPPV based in the remaining EEA region to continue distributing drug products in both markets, although draft legislation issued by the UK government indicates that there may be a transitionary period of 21 months for establishing a UK QPPV, even in the event of a no-deal Brexit.
- Simon Ashworth, VP EU QPPV, EU Head Compliance and Marketed Products and Head PV Affiliate Relations, Takeda
This is an important gathering in the UAE for key representatives from the pharmaceutical industry and I hope to pass on my expert knowledge in QPPV to help improve compliance with pharmacovigilance requirements.”
She has 27 years of industry experience including serving as a Deputy QPPV. Ms.
Much expectation, and responsibility, has been put on the shoulders of the Qualified Person for Pharmacovigilance (QPPV).