On-Site Workshop: Entering the Medical Device Industry: A Practical Guide for Raw Material & Component Suppliers

The medical device industry is known for its stringent standards, continuous innovation, and strong potential for growth. As regulatory requirements evolve, both new and established suppliers must remain agile to maintain compliance and a competitive edge.

This full-day workshop is designed for suppliers of raw materials and components who are either entering the medical device sector or seeking to strengthen and update their existing quality and regulatory systems.

Participants will gain practical insights into:

• Transitioning or aligning from ISO 9001 to ISO 13485
• Understanding the upcoming changes to USP Class VI
• Applying risk-based strategies for biocompatibility and chemical testing
• Meeting evolving regulatory and quality system requirements

Led by experienced industry professionals, the workshop offers a structured, hands-on approach to navigating the complexities of medical device regulations. In addition to foundational content for newcomers, dedicated sessions will focus on current updates, trends, and best practices for experienced suppliers.

Whether you are exploring new opportunities within healthcare or looking to refresh and optimise your existing processes, this workshop will provide you with the tools and knowledge to ensure continued compliance, product safety, and long-term success in the medical device market.

Workshop language: English

Workshop Fee: 250 € (VAT excluded)

For any information please contact us at: Medical-Device@bpt.eurofinseu.com