10 July 2025 Fix the disconnect before it costs you: integrate processes, people & information Organized by Scilife
8 July 2025 Now launching: meet Scilife’s Design & Development tool for medical devices Organized by Scilife
26 June – 26 July 2025 Key considerations before migrating your documentation to an eQMS Organized by Scilife
24 April 2025 Live webinar: Cohort building: real-world applications from AstraZeneca & Boehringer Ingelheim
10 April 2025 Scilife Training | From CSV to CSA: Streamlining software validation with a risk-based approach Organized by Scilife
3 April 2025 Scilife AMA Session | How to survive and thrive in FDA and EU inspections for GxP - Ask the expert Organized by Scilife
27 March 2025 Scilife Showcase | Avoiding FDA Form 483: Streamlining supplier qualification with Scilife Organized by Scilife
20 March 2025 Scilife Training | How to win buy-in for quality investments with a soft skills approach Organized by Scilife
14 November 2024 FREE IP Café - IP Protection of software / computer simulations – Recent developments in European practice
24 October 2024 Medical Device Software Webinar Series - Part 5: Technical Documentation Essentials for Medical Device Software
17 October 2024 Medical Device Software Webinar Series - Part 4: Integrating Clinical Needs into Design & Documentation
8 October 2024 Medical Device Software Webinar Series - Part 3: A unified MDSW development cycle that covers all requirements
