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Medical Services
· MDD - Medical Products
· In-Vitro-Diagnostic (IVD)
· Active Implantable Medical Devices
· Certification of Quality Systems
Quality is a Matter of Life and Death.

Doctors and medical professionals deal with sophisticated medical products on an everyday basis. Under European Community guidelines for medical products, manufacturers whose products have a high-risk classification must establish a link with a "Notified Body". This can be achieved through product testing and/or auditing of the manufacturer's quality management system.

TÜV Rheinland Group is such a "Notified Body" for all medical products. It certifies products and QM systems for the European Market, and also serves as Certification Body for non-European countries.

If you have any more questions, then please contact us! We are looking forward to hearing from you!

 

 







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Related Services
. International Product Approval
. CE Marking

European Directives
. Medical Device Directive 93/42/EEC
. Active Implantable Medical Device Directive (AIMD) 90/385/EEC

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