If you are manufacturing medical devices in the higher risk categories, then it is almost certain that the most cost-effective route to conformity will include having a quality management system meeting one of the Annexes of the relevant European Directive
 
 
What is known as the ‘Full Quality Assurance System’ in the Directives is broadly equivalent to EN ISO 13485:2012 ‘Medical devices, Quality management systems, Requirements for regulatory purposes’, with the addition of certain administrative requirements.
 
 
GEMAR can help your company achieve certification to ISO 13485 and compliance with the relevant directive Annex, providing audits, pre-inspection reviews, gap analyses and quality system development. Feel free to contact us for further information.