MHRA Pharmacovigilance Symposium 2015 is aimed at drug safety representatives from the pharmaceutical industry and academic and quality research organisations who want to:
- understand how to avoid common deficiencies in inspections by learning from the experiences of others
- to gain a greater understanding of new and existing pharmacovigilance requirements
- to understand MHRA expectations in order to improve their organisations’ compliance with pharmacovigilance requirements
Who should attend?
The event is relevant to anyone working in pharmacovigilance across all types of organisations, including:
- EEA Qualified Persons responsible for pharmacovigilance (QPPVs)
- consultants
- contractors
- drug safety representatives from the pharmaceutical industry and academia and representatives from regulatory affairs departments
from Announcements on GOV.UK http://ift.tt/1v9nLso
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