2026 - Medical Device Validation Solutions for Evolving Industry Needs
Date2026-01-21
Deadline2026-01-21
VenueONLINE-VIRTUAL, USA - United States 
KeywordsLife Science; Medical Device; Medical Device Design
Topics/Call fo Papers
The use of computer systems in medical device manufacturing has rapidly expanded, creating a growing need for modernized validation approaches.
This webinar explores digital computer system validation (CSV) approaches for medical device companies and how teams can build processes to meet the industry’s emerging needs.
This session will also outline why traditional validation is shifting, how digital processes address emerging needs and the potential roadblocks to successful transformation.
Digital validation approaches support consistency, reduce redundant effort and help align processes with current regulatory thinking.
The featured speakers will discuss the influence of Computer Software Assurance (CSA), how CSA is prompting a reassessment of long-standing validation methods and key considerations for medical device leaders evaluating digital adoption.
This session will provide clarity on how digital validation strengthens compliance and supports scalable, future-ready processes for medical device teams.
Register for this webinar to learn how medical devices benefit from modern digital validation strategies.
Keywords: Commercial Manufacturing, Medical Device, Medical Device Design, Medical Device Development, Medical Device Innovations, Medical Device Manufacturing, Other Software, Quality, Regulatory, Validation
This webinar explores digital computer system validation (CSV) approaches for medical device companies and how teams can build processes to meet the industry’s emerging needs.
This session will also outline why traditional validation is shifting, how digital processes address emerging needs and the potential roadblocks to successful transformation.
Digital validation approaches support consistency, reduce redundant effort and help align processes with current regulatory thinking.
The featured speakers will discuss the influence of Computer Software Assurance (CSA), how CSA is prompting a reassessment of long-standing validation methods and key considerations for medical device leaders evaluating digital adoption.
This session will provide clarity on how digital validation strengthens compliance and supports scalable, future-ready processes for medical device teams.
Register for this webinar to learn how medical devices benefit from modern digital validation strategies.
Keywords: Commercial Manufacturing, Medical Device, Medical Device Design, Medical Device Development, Medical Device Innovations, Medical Device Manufacturing, Other Software, Quality, Regulatory, Validation
Other CFPs
- Enhancing Signal Detection and Mitigating Placebo Response in Major Depressive Disorder Clinical Trials
- Navigating the Animal Rule in Drug Development with Modeling & Simulation
- Enhancing Clinical Efficiency Through Master Protocol Trial Design
- Improve Effectiveness of Cardiac Assessments in Early Phase Trials with Early Precision QT and AI-powered Data Quality Checks
- Bioassay Method Transfer Strategies to Reduce Variability
Last modified: 2025-12-09 06:46:46
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