Which seminar topics can you find at en.co.tec?
Medical devices are subject to strict requirements, that demand a great deal from companies, their management, and in terms of product testing and quality. Continuous innovation, flawless quality management, and compliance with a wide range of standards are essential—numerous critical points must be addressed before a medical device can be approved.
We at en.co.tec support you in this process! We come from the practice and prepare you for the practice!
A wide range of offerings for all specific requirements for medical devices and in vitro diagnostics
- Training on the Medical Devices Act
- Norms and EU Regulations
- Clinical Evaluation and Studies
- Product Development
- Risk management ISO 14971
- Quality Management ISO 13485
- Creation of Technical Documentation for Medical Devices
- Responsibilities of the Person Responsible for Regulatory Compliance (PRRC) under MDR/IVDR
- and many other topics
