Regulatory Affairs Manager appointed as Corporate PRRC responsible for fulfilling requirements as per article 15 of the EU Medical Device Regulation (EU) 2017/745 (MDR).
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BROWN Richard
Vice President of Quality Assurance and Regulatory Affairs appointed as Corporate PRRC responsible for top level management ensuring that the company is fulfilling requirements as per article 15 of the EU Medical Device Regulation (EU) 2017/745 (MDR).