Meet MedReg at MEDICA + COMPAMED 2026
- 16–19 November 2026
- Messe Düsseldorf, Düsseldorf, Germany
- Booth to be announced
Reserve a 30-minute slot
Pick a day and time. All times are CET (UTC+1), Düsseldorf time. We confirm every request by email and share the exact meeting point once our booth is announced.
- 1 Day
- 2 Time
- 3 Your details
Choose a day
Choose a 30-minute slot CET (UTC+1), Düsseldorf time
Select a time above to continue. Slots are confirmed by our team by email.
30-minute 1:1 sessions
A focused, free conversation about your device and target markets.
Senior regulatory experts
Talk directly to the people who prepare and submit the documentation.
Clear next steps
Leave with the regulatory pathway, the documents you need and a realistic plan.
What we can discuss
Regulatory support for every market
Bring your device questions. We cover approvals and compliance for Europe, the USA, global markets and India.
Europe Regulatory Services
- EU MDR 2017/745
- EU IVDR 2017/746
- CE marking
USA Regulatory Services
- US FDA 510(k)
- 21 CFR Part 820 (QMSR)
- UDI / GUDID
QMS & Global Regulatory Services
- ISO 13485:2016
- MDSAP
- ISO 14971
India Regulatory Services
- CDSCO
- Medical Devices Rules, 2017
Who should book a meeting
- Medical device manufacturers
- Diagnostics and IVD companies
- Component and contract-manufacturing suppliers
- Distributors planning market entry
Photo: Düsseldorf Media Harbour – Greg Zaal via Poly Haven (CC0)
