Advice on - Import export

Our experts support you with the following services: - Toxicological assessment within the framework of the REACH and biocide regulations - Environmental Risk Assessment (ERA = Environmental Impact Assessment), e.g. for pharmaceuticals - Literature research and evaluation - Examination of the reliability and validity of the studies carried out (according to OECD guidelines, EU methods or according to Klimisch et al. 1997) - Assessment of relevant toxicological endpoints, e.g. acute toxicity, genotoxicity, irritation / corrosion of the skin or eyes - Evaluation of all relevant toxicological, ecotoxicological endpoints, e.g. freshwater organisms (daphnia, algae, fish) - Read Across - Study monitoring of studies - Creation of the Endpoint Summaries and Endpoint Study Records for IUCLID (REACH and biocidal active ingredients and products) - Safety assessment and safety report for cosmetic products - Water hazard class - etc. Questions?--> contact@invitro-connect.com

Material Safety Data Sheet - Hazardous Substances Advice and Hazardous Substance Management Overview of our services: - Check of conformity and plausibility as well as updating of existing Material Safety Data Sheets - Preparing of extended Material Safety Data Sheets - Classification and labelling of substances according to the current GHS regulation (CLP regulation) Depend on requirements INVITRO-CONNECT GmbH checks whether your existing safety data sheets are still compliant and plausible to follow latest REACH guidelines and if necessary, updates them for you. Furthermore, based on our know-how we provide extended material safety data sheet, following the REACH Directive as well as the latest European GHS regulation for classification and labelling of substances. INVITRO-CONNECT GmbH - Fast Project Execution: personal - competent - reliable --> contact@invitro-connect.com Best regards Pascal Piller and Dr. Ute Hassmann and the whole team of INVITRO-CONNECT GmbH

Material Safety Data Sheet - Hazardous Substances Advice and Hazardous Substance Management Overview of our services: - Check of conformity and plausibility as well as updating of existing Material Safety Data Sheets - Preparing of extended Material Safety Data Sheets - Classification and labelling of substances according to the current GHS regulation (CLP regulation) Depend on requirements INVITRO-CONNECT GmbH checks whether your existing safety data sheets are still compliant and plausible to follow latest REACH guidelines and if necessary, updates them for you. Furthermore, based on our know-how we provide extended material safety data sheet, following the REACH Directive as well as the latest European GHS regulation for classification and labelling of substances. INVITRO-CONNECT GmbH - Fast Project Execution: personal - competent - reliable --> contact@invitro-connect.com Best regards Pascal Piller and Dr. Ute Hassmann and the whole team of INVITRO-CONNECT GmbH

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