Whitepaper
Validation strategies in medical devices
In this whitepaper you will learn:
- Why audit readiness tops budgets & remote audits
- Where med device teams see ROI from digital tools
- How CSA adoption is progressing across industry
- Where AI pilots & use cases make sense
- Five clear actions to guide your 2025 roadmap
VALIDATION STRATEGIES
2025 roadmap for medical device validation
This whitepaper is your 2025 roadmap to strengthen medical device validation practices, streamline operations, and stay ahead of rising audit demands. Explore new benchmarks on team structures, outsourcing, and budgets, plus the latest on digital adoption, CSA implementation, and early AI pilots. Gain five practical recommendations to improve efficiency, data integrity, and continuous compliance in this complex regulatory environment.
Industry-leading validation
Kneat is trusted by 8/10 world’s largest life sciences companies to provide digital validation and GDP solutions across their entire manufacturing lifecycle.
Uncompromised data protection
We protect data integrity across the entire validation lifecycle with password protected signatures, automatic timestamps, and a comprehensive audit trail.
Maximize efficiency
Kneat is proven to reduce validation cycle times by 50% across multiple validation disciplines through online test execution, remote approval, and more.
Seamless audit preparation
We set you up for audit success from the start with automatic audit trails and easy paperless handovers to make it easier for audits and remote inspectors.
Validation strategies in medical devices
Download the 2025 State of Validation whitepaper for med device benchmarks.
Download whitepaper