- Date: Jul 08, 2026
- Location: Virtual
Join us for this live partner-hosted webinar!
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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