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
25 September 2025 Next Horizons in Drug Discovery: From Research to Clinic Organized by Sino Biological Europe
23 September 2025 PMS & PMCF Compliance for Medical Devices Under EU MDR: Webinar 2 Organized by QbD Group
23 September 2025 From Ambition to Action: Strategy workshop for medtech & digital health companies Organized by Biovia
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
9–12 September 2025 Methods and applications for single-cell and spatial multi-omics Organized by KU Leuven Institute for Single Cell Omics – LISCO
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
