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European Union Device Regulation (EU MDR)
The EU MDR replaces the MDD and expands the requirements for conformance.
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Edwin Waldbusser
Regulatory Consultant , Med Device Advisors, Founder,Medical Device SOP Advisors,LLC-offering 82 SOP's,The EU MDR replaces the MDD and expands the requirements for conformance.
View DetailsIn this webinar you will learn how to prepare for an inspection and how to respond to a 483 or Warning letter if you receive one.
View DetailsAI/ ML will revolutionize medicine by making diagnosis and treatment more accessible and more effective.
View DetailsThis Webinar will explain what 21 CFR Part 11
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