Scilife Training | From CSV to CSA: Streamlining software validation with a risk-based approach
Validation shouldn’t feel this hard… right? Too much paperwork. Slow processes. Constant compliance changes. We get it—and we’re here to help.
Join Scilife's free webinar to learn how FDA’s CSA principles can help you embrace a risk-based, agile methodology.
🎤 Featuring Harsh Thakkar, CSV expert & CEO of Qualtivate.
Validating a new system can be a major headache—resource-intensive, heavy on documentation, rigid, and tough to navigate.
We get it. After hearing your challenges, we're hosting a webinar to help revamp your approach with the FDA’s emerging Computer Software Assurance (CSA) principles into your system validation and vendor management programs.
We’ll show you how to:
- Transition from traditional CSV to a lean, risk-based CSA approach
- Apply smart testing strategies for speed and reliability
- Leverage vendor data to cut duplication
- Integrate continuous monitoring and automation for faster issue resolution
- Optimize your QMS for improved team collaboration
You’ll hear from Harsh Thakkar, CEO and Founder of Qualtivate, and a CSV expert who helps life sciences companies enhance their quality management and develop innovative technologies.
Angel Buendía, Scilife’s Knowledge Manager, will be moderating this online session.
📅 April 17th, 2025 | 11:00H (CET)
No fluff, just what you need. This practical, hands-on webinar will show you how to implement a risk-based, agile approach that actually works.