From Concept to Compliance - Streamlining Medical Device Development, Manufacturing and Regulatory Pathways

The development and market launch of medical devices is a complex process that combines technical innovation, regulatory requirements and economic factors. From the initial idea to successful approval, manufacturers must overcome numerous challenges to ensure safety, efficacy and market conformity.

This presentation will highlight practical strategies for optimized product development, efficient manufacturing and successful approval in accordance with current regulatory requirements. The focus will be on efficient development approaches, agile methods, early regulatory involvement and the use of digital tools for documentation and traceability.

Practical examples illustrate how smart planning, and interdisciplinary collaboration can shorten development times, reduce costs and at the same time ensure quality and compliance with regulatory requirements.

Please note: 

• Access to the MedtecLIVE Innovation Expo and participation in its supporting program is only possible with a valid congress ticket. Tickets are available here.
• The presentation will be held in English.