Medical Device Verification & Validation is a conference dedicated to harnessing process validation to reduce risk and ensure overall product quality.
Topics
- Implement a sturdy VMP to assure product quality
- Integrate risk management with V&V for greater product safety
- Incorporate earlier processes in order to promote cost reduction, fewer errors, and faster market time
- Leverage different tools and technologies for improved process validation activities
- Interpret changes to the EU MDR in order to ensure optimal compliance
Who should Attend
Senior attendees with responsibilities in:
- Design Verification and Validation
- Verification & Validation
- Process Engineering / Verification
- R&D
- Regulatory Affairs & Compliance
- Quality Assurance / Control
