MDD 93/42/EEC services
-
STEMart - Notified Body (EU) Services
CE marking is the manufacturer's declaration that their product complies technically and administratively with the essential regulatory requirements of Medical Device Directive 93/42/EEC (MDD) and its supplementary Directive 2007/47/EEC, Active Implantable Medical Devices Directive 90/385/EEC ...
By STEMart based in Shirley, CALIFORNIA (USA). from Medical Device Development Service - Medical Device Certification Services Service line
-
Audits Services
An audit is the most effective method to establish certainty that you as the manufacturer or distributor of medical devices are in the position to meet all requirements. Metecon offers comprehensive support in this regard with a wealth of experience and know-how. Take a moment to get an overview of our services. And if you see any need, we look forward to discussing a solution with ...
By Metecon GmbH based in Mannheim, GERMANY. from Services IVD - Quality Management Service line
Need help finding the right suppliers? Try XPRT Sourcing. Let the XPRTs do the work for you