Production and service provision process in ISO 13485 certification in Qatar?
Clause 7.5 of ISO 13485 certification in Qatar, which offers requirements for manufacturing and provider provision, motives a lot of...
How to write a good ISO 13485 Quality Policy?
When enforcing a Quality Management System (QMS) for your medical device manufacturing organization, you will discover that one of the...
How can ISO 13485 certification help with MDR compliance?
As a medical device manufacturer, if you are implementing man ISO 13485:2016 certification in Qatar Quality Management System (QMS), you...
The importance of quality assurance in disposable medical device manufacture
ISO 13485:2016 Certification in Qatar Quality assurance is essential to all medical devices, which include disposable ones. Should a...
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...
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...
How to select a consultant for ISO 13485 implementation in Qatar?
If your organization has determined to implement the ISO 13485 Certification in Qatar standard, you may be thinking about bringing in a...
