May 13, 2026
MDR 2017/745 TECHNICAL DOCUMENTATION REQUIREMENTS FOR THE ORTHOPEDIC INDUSTRY
This webinar is specifically designed for Legal Manufacturers of Orthopaedic Implants and reusable surgical instruments. A brief introduction on current status and MDR conformity assessment process in TÜV Nord, will be followed by an one-hour presentation inspired by field discussions and concerns of the Orthopaedic Industry. The webinar will cover MDR Technical Documentation requirements and offer participants a valuable insight into all pertinent aspects. The agenda will be followed by a constructive Q&A session which will further facilitate understanding and take-home messages.
