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Chris MacKay
Independent Consultant, Regulatory Affairs at CJM Medical Device Consulting Ltd

Profile


After earning a Ph.D. in Medical Science in 2011, Chris has worked for a number of Medical Device Manufacturers as a Senior RA Specialist and project Team Lead.

Most recently, he has worked as an independent consultant for several large MD manufacturers to successfully transition high risk class technical files, and related deliverables, to the EU MDR.  

https://www.linkedin.com/in/chris-mackay-35357b16/

Agenda Sessions

  • Best Practice to Balance MDD and EU MDR Products

    , 16:55
    View Session

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Amanda Maxwell
Medtech Regulatory Affairs Editor, MedTech Insight, Pharma Intelligence
Informa, UK

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