inmedis is your Swiss partner for quality management and regulatory affairs in the medical device industry. Our experienced experts support you pragmatically and goal oriented in the following areas:- Quality management systems: ISO 9001 / ISO 13485 / FDA QSR / Audits / MDSAP- Interim Quality Management Resources: Outsourcing of QM/RA functions / coaching and support- Technical Documentation: MDR-compliant technical documentation / gap analyzes / reviews- Validation: Design and manufacturing processes / Computer systems (CSV)- Biocompatibility: Planning and implementation / ISO 10993- Regulatory affairs: Approval strategy and registrations / Post-market surveillance and standards monitoring