Comparison of the EU MDR and IVDR regulations
ISO 13485 certification in South Africa with the new EU Medical Device Regulation, many companies want to make certain that they are in...
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How to manage the medical device sterilization process according to ISO 13485:2016?
13485:2016 certification in Qatar Sterilizing medical devices is of crucial value in the scientific sector. Even so, at a range of...
Design and improvement validation and verification in accordance to ISO 13485
Producing any section of a product consists of validation and verification in its layout and development. ISO 13485 certification in Iraq...
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