21 October 2025 The Future of Regulatory Intelligence: Transforming Compliance with Automation and AI Organized by Scilife
16 October 2025 The Artificial Intelligence Agenda from Capitol Hill to State Capitals: Where We Are and Where We Are (Probably) Going Organized by Crowell
7 October 2025 Webinar - Growth in Health: Why Antwerp is the Place to be for Your Health Company Organized by Stad Antwerpen
30 September 2025 What the 2025 EU GMP Revisions mean for digitalization and Artificial Intelligence Organized by Scilife
25 September 2025 Traceability from day one: Smarter design controls with Scilife Organized by Scilife
23 September 2025 PMS & PMCF Compliance for Medical Devices Under EU MDR: Webinar 2 Organized by QbD Group
23 September 2025 Why medical device companies fail with design and development inputs Organized by Scilife
18 September 2025 The eQMS validation process explained: steps, risks, and best practices Organized by Scilife
9 September 2025 PMS & PMCF Compliance for Medical Devices Under EU MDR - Webinar 1 Organized by QbD Group
28 August 2025 Prevent expensive errors and recalls by managing CAPAs proactively Organized by Scilife
26 August 2025 Medical device cybersecurity now: FDA Rules vs EU MDR—are you ready? Organized by Scilife
29 July 2025 Importing your documents into an eQMS: what to expect and how to prepare Organized by Scilife
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
10 April 2025 Scilife Training | From CSV to CSA: Streamlining software validation with a risk-based approach Organized by Scilife
