25 November 2025 When nonconformities strike: how to stay compliant with Scilife Organized by Scilife
4 November 2025 Quality Management System Regulation (QMSR): Key insights and strategies to prepare for the transition Organized by Scilife
28 October 2025 What eQMS implementation really looks like (Spoiler: It’s not that hard) Organized by Scilife
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
14 October 2025 Automated Microscopy and AI-based Image Analysis in Disease Models Organized by Nikon Belgium
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 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
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
