Seminars
Public seminars for the medical device industry are designed in cooperation with the TÜV Rheinland Academy and presented by regular services. Herewith an overview of the seminars we offer in partnership with the TÜV Rheinland Academy.
- Auditor in the medical device industry
- Outsourcing of processes in the medical device industry
- CAPA & CO for medical device manufacturers
- The CE identification process for medical devices
- Design and development of medical devices
- The new European Regulation on Medical Devices (MDR)
- No fear of reportable events in medical devices
- Clinical evaluation of medical devices
- Manager Regulatory Affairs – Medical Devices International
- MDSAP Medical Device Single Audit Program
- Post-Market Surveillance of medical devices
- QM representative (QMR) for medical device manufacturers
- Quality Management System according to 21 CFR 820 (QSR-USA)
- Qualitätsmanagementsystem nach EN ISO 13485
- Quality Management System according to EN ISO 13485
- Regulatory requirements for medical devices
- Risk management according to ISO 14971 / EN ISO 14971
- Statistical methods in the medical device industry
- Technical documentation for medical devices
- Validation of processes in the medical device industry
- Person responsible for regulatory requirements under Article 15 of Regulation (EU) 2017/745 (MDR)