Organic international - Import export

Medical Device Services / Medical Device Laboratory Testing INVITRO-CONNECT GmbH offers you: - General regulatory advice for medical devices - All regulatory examinations and tests under GLP - Project management and study monitoring - Medical Device Regulatory Service - Product testing for contained SVHC substances INVITRO-CONNECT offers you a complete service for the approval of medical devices according (EU) 2017/745 (Medical Device Regulation - MDR) / ISO 10993. From the development of an ideal test strategy to laboratory and project coordination, study monitoring, toxicological expertise and GLP inspections in the cooperation laboratories. We deliver the finalized test reports including the registration dossier - digitally and on paper, worldwide. Benefit from our diverse know-how, our experienced cooperation partners and an international, very well-organized network. Questions? -> contact@invitro-connect.com

INVITRO-CONNECT GmbH: - Regulatory advice - All OECD laboratory tests - Phys-Chem / Tox / in vitro tests / Genotox / Ecotox, E-fate etc. - Personal project management - in-house toxicologists - Study monitoring - Study Summaries, IUCLID 6 - Dossier creation - MSDS etc. Benefit from an international, very well organized network: carefully selected experts, in-house toxicologists and more than 80 accredited test laboratories and service providers with over 20 years of experience in the industry. We are your competent partner for regulatory and toxicological issues, expert services, reports and all OECD laboratory tests We are also happy to be your reliable partner for your laboratory services and regulatory projects. Questions? -> contact@invitro-connect.com Your Mrs. Dr. Ute Hassmann and Your Mr. Pascal Piller