- Webinar
MedTech Validation: Smarter V&V, Design Controls, and Digital Device Files
Strategies for aligning verification, validation, and product lifecycle documentation
- July 8, 11:00 AM - 12:15 PM EST
MedTech Validation: Smarter V&V, Design Controls, and Digital Device Files
Strategies for aligning verification, validation, and product lifecycle documentation
July 8, 11AM – 12:15 PM EST
Medical device organizations face increasing pressure to modernize V&V programs, streamline design control documentation, and support digital DHF/DMR systems. This webcast highlights the most important shifts influencing MedTech validation in 2026, including risk-based testing, connected device considerations, and evolving expectations for software and algorithmic components.
What You’ll Learn:
- V&V strategies that reduce testing burden while maintaining compliance
- Updates affecting design controls and documentation workflows
- Best practices for building and maintaining digital DHF/DMR systems
- Software validation and SaMD considerations
- Human factors and usability trends in modern design
- Risk-based and lifecycle-driven validation techniques
- Common gaps found during MedTech inspections
- Approaches to managing product updates and change impact
Who Should Attend:
MedTech validation teams, design and development staff, quality engineers, regulatory affairs, R&D leaders, and device manufacturing professionals.
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July 8
11:00 AM - 12:15 PM EST
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