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On the 18 April, we will be running a one day workshop (9.30am to 4.30pm) to discuss the impact of Brexit on the Pharmaceutical Quality System. The pharmaceutical industry has already undergone significant change as a result, and many pharmaceutical supply chains have already changed in anticipation. However, there is much still to be decided, from the implementation of security features to the acceptance of UK medicines by the EU with/without recertification/retesting.
The question is…. what is next? Join us for a discussion on the implications once the deal is in place.
Suitability
This is a must attend workshop for trainee QPs, practising QPs and Quality professionals.
This one day workshop will allow you to:
Review the requirements for product and site licenses for medicinal products (human and veterinary) and clinical trials
Clarify the impact of the status of the UK as a third country in relation to the EEA
Identify which quality systems are impacted
Define the role of the QP GMP and QPPV in the UK
Discuss the different possible options with other quality professionals
