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REGISTRATION FORM Advanced Pharmacovigilance Auditing # 18551 911 April 2018 Hilton Canary Wharf London, United KingdomREGISTRATION FESTERS AND CONDITIONSRegistration fee includes refreshment breaks,
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What is advanced pharmacovigilance auditing 18551?
Advanced pharmacovigilance auditing 18551 is a process of evaluating and monitoring drug safety data to ensure compliance with regulatory requirements.
Who is required to file advanced pharmacovigilance auditing 18551?
Pharmaceutical companies and drug manufacturers are required to file advanced pharmacovigilance auditing 18551.
How to fill out advanced pharmacovigilance auditing 18551?
Advanced pharmacovigilance auditing 18551 can be filled out electronically through the designated regulatory authority's online portal.
What is the purpose of advanced pharmacovigilance auditing 18551?
The purpose of advanced pharmacovigilance auditing 18551 is to ensure the safety and efficacy of drugs on the market by monitoring adverse events and taking appropriate actions.
What information must be reported on advanced pharmacovigilance auditing 18551?
Information such as drug safety data, adverse events reports, risk management plans, and compliance with regulatory requirements must be reported on advanced pharmacovigilance auditing 18551.
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