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Posts Tagged Medicines Act

Does the new SI 2012:1916 change the requirement for QP practical experience under Specials Licenses?

A question I was asked recently is whether the change to the UK legislation, you know the one, the reduction in the bulk of the 1968 Medicines Act and revoking approx 200 Statutory Instruments to replace them with the new sleek and streamlined SI 2012:1916, affects the

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Latest QP Question

What are the requirements for unlicensed medicinal products in the UK, do you need QP certification? Where would you find guidance?

Latest QP Scenario Practice

Iron Oxide - used as an excipient in many of your products. You find that the supplier has been irradiating the material without your knowledge. What implication does this have for your product? What does this mean for the effectiveness of your supplier oversight and PQS?


"The knowledge, guidance and advice provided by Alex was excellent. Alex has first hand knowledge of the requirements needed for candidates to be successful QPs and provides a level of training to meet these requirements. I can highly recommend QPQuandry as a service provider"
Alex Hern, Sanofi.


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