Learn more about some of the common and potential points of vulnerability with commercial as well as safety and reputational implications, and what companies can do to reduce those risks.
TORONTO (PRWEB) November 23, 2020
When the current European pharmacovigilance (PV) legislation came into force in Europe in 2012, pharmaceutical companies targeting the region had to put in place a number of formal measures to monitor the safety of products and any issues once those products were being marketed in the real world.
These measures also mandate that life sciences companies must run, check and document their PV activities so that regulatory authorities can be confident that standards are being upheld and that nothing is being missed.
This means pharmaceutical organizations must be able to provide evidence of strong standard operating procedures on demand, and that includes measures implemented down the supply chain. Yet, even today, companies are still struggling to fulfill their obligations, causing marketing authorization holders (MAHs) to fail inspections, incur fines and see products withdrawn from markets.
Join expert speakers from Arriello, Vanessa Fachada, Pharmacovigilance Manager and EU QPPV; and Peter Kohut, Director of Drug Safety and EU QPPV, in a live webinar on Thursday, December 10, 2020 at 11am EST (4pm GMT/UK) to learn more about some of the common and potential points of vulnerability with commercial as well as safety and reputational implications, and what companies can do to reduce those risks.
For more information, or to register for this event, visit Pharmacovigilance Audit Failures: What’s Still Going Wrong?
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