CE-Immundiagnostika is a manufacturer certified to European quality standards whose manufacturing processes comply with GMP guidelines.
Since the founding of the company in 1979 we have operated as a reliable and high-quality manufacturer for pharmaceutical companies and specialised supplies of clinical diagnostics.
We have been ISO-EN 9001 certified for production, distribution, and development since 1996 and audited by TÜV for ISO 13485 according to the In Vitro Diagnostic Directive EC 98/79 of the European Parliament and the Council since 2002.
We owe our success to the profound knowledge of our entire staff based on extensive practical experience and our certified technological production environment.
CE-Immundiagnostika is interested in finding partners/companies for distribution of its Blood Typing Reagents worldwide.