Save the date – A half-day event for MedTech startups and scale-ups preparing for clinical investigations
We’re happy to invite you to a hands-on morning session focused on essential – and often overlooked – parts of the clinical development journey before CE-marking.
What we’ll cover
- Early Clinical Strategy – What must be in place before you apply for a Clinical Investigation
- Study design – From concept to statistically sound setup
- Biocompatibility in Practice – Getting it right from the start
- Data handling – Planning for structured collection, storage, and analysis
- Notified Body expectations – What NBs expect from your clinical evidence
Who should attend
Early-stage MedTech companies in the clinical phase, especially those preparing for first-in-human investigations or validation studies. The session is tailored for startups and scale-ups with limited in-house resources for clinical development.
📅 Date: Thursday, 18 September
🕗 Time: 08:00–11:45
📍 Location: GoCo, Gothenburg
🎁 Cost: Free of charge
Hosted by: GBA Key2Compliance
With expert contributions from: APNC, MediCase, and TÜV SÜD