Events

• Events

• February 21, 2025
• | English

Join us for an insightful webinar on Pharmacovigilance (PV) audits. This session will cover key audit stages, common challenges, and frequent findings, ...

• Events

• March 20, 2025
• | English

Join us for an insightful webinar on EU Regulation 2024/1860. You'll learn about strategies to navigate new regulatory challenges; best practices for risk ...

• Events

• March 24, 2025
• | English

Documents Medical Device Classification Poster Free Workshop: Preparing For Your Medical Device's Regulatory Strategy Plan Bringing a medical device to market ...

• Events

• March 24, 2025
• | English

Join us for an insightful webinar on building an LSO program. As global pharmacovigilance regulations grow more complex, having a strong LSO program is ...

• Events

• March 26, 2025
• | English

Join our webinar about Market Access Strategy for Device Reimbursement in Europe and discover the key elements of crafting a successful market access strategy ...

• Events

• April 07, 2025
• | English

Join our webinar about Performance Evaluation of In Vitro Diagnostics and discover how manufacturers can demonstrate clinical evidence efficiently, with a ...

• Events

• April 16, 2025
• | English

This session provides pragmatic guidance on how to establish risk and overall residual risk acceptability, and how to perform a clear, structured benefit-risk ...

• Events

• April 17, 2025
• | English

With the EU Clinical Trial Regulation (EU No. 536/2014) fully in force, safety reporting has become more centralized, more visible, and less forgiving. Whether ...

• Events

• April 22, 2025
• | English

Join our webinar about EU AI ACT and discover how it will shape the digital future of the healthcare sector, impacting medical device manufacturers and driving ...

• Events

• April 24, 2025
• | English

Meet ProductLife Group at RAPS Euro Convergence 2025 Booth 17 | Square Brussels Meeting Centre | 13-16 May Your Regulatory Partner: from Strategy to Submission ...