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Rapid Regulatory Compliance Clinical Part 1 Form

Rapid Regulatory Compliance Clinical Part 1 Form

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hi there are you looking for more information on how to fulfill the requirements of the person responsible for Regulatory Compliance ing to the MDR in a practical way then you have come to the right place my name is Ponte Sierra and I am the author of the online course introduction to person responsible for Regulatory Compliance I have worked in the medical device industry for over 20 years and my interest for Regulatory Affairs brought me to the world of notified bodies in 2014. the notified body I worked for was designated for um MDR under my management and I am also an MDR lead auditor taking this short course will give you a better understanding of the prrc role on a high level and hopefully get you interested in taking the full prrc online course remember it's mandatory for all manufacturers to have a prrc available if you are CE marking Medicaid devices ing to the MDR the prrc requirements also applies to any European representative for those manufacturers needing that me

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