Streamlined Risk Management: Adapting to new ISO/FDIS 10993-1 requirements

Are you prepared for the latest updates to ISO/FDIS 10993-1?

This full-day, in-person workshop offers a deep dive into the recent changes to the ISO 10993 series, which could significantly impact the biological safety assessment of medical devices.

Join industry experts to explore:

• The key adjustments required to meet the new standard
• How to identify and close gaps in your current data set
• Relevant testing and evaluation methods
• Practical application of ISO 14971 principles for risk analysis and management

Whether you're working in regulatory affairs, quality assurance, or product development, this workshop will provide the knowledge and tools needed to confidently implement the new requirements and ensure compliance.

Workshop Language: English

Registration fee:  €250, VAT Excluded

For any information you can contact us at: medical-device@bpt.eurofinseu.com