Date: 16-20 June, 2025
Location: MOA Berlin, Berlin, Germany
Language: English
Introduction
Join the 2025 MedTech Summit and gain comprehensive insights for Medical Device and IVD Manufacturing.
Qserve Experts will be presenting during the following sessions:
Day 1 – Monday 16 June
- Chairperson’s Opening Remarks: SME Survival Guide with Robert Paassen starting at 08:40
- Market Analysis with Robert Paassen starting at 08:50
- Introduction to the Medical Devices Regulation (MDR) and In Vitro Diagnostic Devices Regulation (IVDR) with Robert Paassen starting at 09:35
- Supplier Selection and Engagement with Robert Paassen starting at 11:10
- Phases of QMS with Robert Paassen starting at 11:55
- Chairperson’s Afternoon Remarks: SME Survival Guide with Robert Paassen starting at 14:10
- Technical File and Strategy Preparation with Robert Paassen starting at 14:15
- Ask Us Anything! With Robert Paassen starting at 17:00.
Day 2 – Tuesday 17 June
- Panel: Coping with Cross Legislation: Looking Beyond MDR with Gert Bos starting at 08:10
- Biomarker Testing in Pharmaceutical Clinical Trials: The Good, Bad and Gray with Kristiane Schmidt starting at 09:25
- Panel Discussion: Inducing Innovation: The Regulatory Landscape and Access Pathways with Bianca Lutters starting at 11:10
- Panel: EU MDR Common Questions – The Answers! with Gert Bos starting at 17:00
Day 3 – Wednesday 18 June
- Workshop Leader Opening Remarks with Gert Bos starting at 08:30
- Chairperson’s Afternoon Remarks: EU AI Act Workshop with Gert Bos starting at 14:10
- Collecting Clinical Evidence with Gert Bos starting at 14:20
- Post-Market and Vigilance Requirements with Gert Bos starting at 15:05
- Practical Example: Certifying Devices under the EU AI Act with Gert Bos starting at 16:15
Day 5 – Friday 20 June
- Collecting Clinical Data for AI/ML Devices & Diagnostics with Bianca Lutters starting at 13:30
For more information and to register for the event, visit the MedTech Summit event website.
Qserve Attendees: