Virtual Training | Person Responsible for
Regulatory Compliance (PRRC)
Training
📅 Date: 20 and 27 February, 2025
📍 Location: Virtual
Qserve offers specialized PRRC training, aligned with MDR/IVDR requirements and MDCG 2019-07 guidance, with an option to obtain a personalized certificate demonstrating your qualification for Notified Body audits.
Live Webinar | Decoding the EU AI Act:
Latest Insights and Evolving Interpretations
Webinar
📅 Date: 4 March, 2025 ⏰ Time: 16:00 – 17:00 CET
Join our webinar to explore the impact of the EU AI Act on medical devices and IVDs, with expert insights on efficient compliance strategies, a 45-minute presentation, and a live Q&A session.
Join Qserve experts at the 2025 RAPS Euro Convergence, Europe’s premier regulatory affairs conference covering the latest in medical devices, IVDs, pharmaceuticals, AI, software, and more.
Qserve is proud to be part of this premier event with:
A Dedicated Booth (Booth 30): Stop by to discuss your regulatory and clinical needs, explore our services, and learn how we can support your needs.
Engaging Presentations: Join Qserve Experts in seven presentations during the event. Visit our website for the full speaker program.
This is your opportunity to connect with industry leaders, explore groundbreaking advancements, and contribute to the future of clinical trials. Gert Bos, Maria Cámara Torres, Keith Morel. Kristiane Schmidt and more look forward to seeing you there!
Live Webinar | Strategies for Collecting
High-Value Data for Regulatory Success
Webinar
📅 Date: 4 March, 2025 ⏰ Time: 16:00 – 17:00 CET
Join our live webinar, co-hosted with Viedoc, on strategies for collecting high-value data for regulatory success, featuring a 45-minute presentation and a live Q&A session.
Missed our Most Recent Webinar on Essential Tips & Tricks for Launching a Clinical Study under MDR
Watch our on-demand webinar with Armêl Plaine for practical tips and real-world strategies to navigate EU clinical trial regulations and ensure trial success.
