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29 March
The Routes To Conformity - Navigating EU Regulation Conformity Assessment Procedure for Medical Device under the Responsible Model (EU MDR 2017/745 & EU IVDR 2017/746). A medical device manufacturer has to follow Conformity Assessment Procedure bef...  Offering
28 March
Integrated Quality Management System: Your Complete Solution Experience seamless quality control with our Integrated Quality Management System. Elevate efficiency and productivity effortlessly. The QMS requirements of the Canadian Medical Devices Regulations ar...  Offering
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