HEATKEYS

We provide rigorous quality management reviews and product certifications for medical device manufacturers around the world, and we can do it for you too. Get advice and a free e-update service from BSI Medical Devices.

CE mark for medical devices, ce mark for machinery, ce mark technical file, EU authorized representative for medical devices and machinery. ISO 13485 for medical device manufacturers. FDA 510(k) service. FDA US Agent for non-us medical device manufa...

LNE / G-MED:CE Mark medical devices and directives, certification ISO 13485, ISO 9001, ISO training / testing, AIMD, IVDD, Canadian medical device regulations. CE Mark medical devices and directives, Canadian / European medical device regulations, ce...

FAQ answered by Wellkang for Medical Devices CE marking (mark): What is EU/EC European Authorized Representative (Authorised Representative)?

The National Standards Authority of Ireland is a registrar and Notified Body providing quality system, medical device and aerospace certifications.

CFPIE.com is a leading provider of pharmaceutical training offering many biopharmaceutical courses. We offer over 120 courses for pharmaceutical, biotech and medical device Professionals.