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Medical Devices


For Application/Request for Quote to ISO 13485:2003 click here

For Application/Request for Quote to ISO 13485:2003/CMDCAS click here

For CE Marking Applications, Substantial Change, Non-Substantial Changes and links to Directives click here

Medical device manufacturers are subjected to many regulatory systems,
international and national standards. This regulatory environment is constantly
changing and influenced by many national and international forums and particularly
the drive towards global harmonisation. NSAI is uniquely positioned to interpret
the EU and global situation and guide on the emerging requirements and regulations.

 

Contact:

Dr John O'Dwyer

Ph: 091 771943
Email: john.odwyer@nsai.ie

Jacinta Kenneally

Ph: 01 8073929
Email: jacinta.kenneally@nsai.ie




Last Updated - [04 Nov 2008 @ 15:00:48]

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