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13 June
The key differences between MDR and IVDR in the EU In the European Union (EU), two significant regulations have been introduced to enhance the safety and effectiveness of medical devices – the In Vitro Diagnostic Regulation (IVDR) and the Medical De...  Offering
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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