QA/RA consultancy for Medical Devices

At the moment, no services are available

· E marking for Medical Devices (Medical Device Directive 93/42/EEC)

· Quality System Implementation (ISO9001/13485 & FDA 21 CFR 820)

· Quality Management a.i.

· Audits: internal and external

· Process improvement / optimizing Quality Systems

· Technical Documentation / Device Master Records

· Education & Training

Contact:

J. Six Dijkstra

Leeuwerikstraat 31

3443 AX Woerden

tel.:  +31-(0)6-13212942

KvK-nr:  30237594

Btw-nr:  NL.1761.577.85.B01