RAPS's recurring EU Medical Device Regulation 2017/745 workshop returns , held virtually — a practice-focused walk through updating a quality system, overseeing economic operators, labeling and technical documentation under the EU MDR, built around worked examples rather than a line-by-line regulatory read-through.
Dates and format
- Dates: 2–5 November 2026
- Format: virtual, live online program
- Organizer: Regulatory Affairs Professionals Society (RAPS)
- Fee: $1,125 members / $1,290 non-members
What it covers
RAPS pitches the workshop as practical rather than introductory: updating a quality system to EU MDR requirements, overseeing economic operators (importers, distributors and authorized representatives), getting labeling right, and handling technical documentation — each walked through with worked examples rather than a straight read of the regulation's text.
Who should attend
Regulatory affairs and quality professionals who already have MDR exposure and need working fluency — the level RAPS pitches this at assumes some prior contact with the regulation rather than a first introduction. Attending RAPS's broader Convergence program the following September carries dedicated MDR/IVDR sessions too, and RAPS Regulatory Intelligence Conference Europe runs the same week in Barcelona for teams building out a European regulatory presence.
Frequently asked questions
When is RAPS's EU Medical Device Regulation 2017/745 workshop?
The next session runs 2-5 November 2026, held virtually. RAPS repeats this workshop several times a year; this is the November 2026 offering, last confirmed on 21 September 2026.
Is the workshop in person or virtual?
Virtual. RAPS runs this as a live online program rather than an in-person session.
How much does it cost?
RAPS lists $1,125 for members and $1,290 for non-members, per its event page as of 21 September 2026. Confirm current pricing before registering.
What does the workshop cover?
RAPS describes practical guidance on updating a quality system, overseeing economic operators, labeling and handling technical documentation under EU MDR 2017/745, with worked examples rather than a line-by-line regulatory read-through.
Who should attend?
Regulatory and quality professionals still building working fluency in the EU MDR — the workshop is pitched at practical application of the regulation, not an introductory overview.
Sources & further reading
- RAPS. Workshop: EU Medical Device Regulation 2017/745 (November 2026) — dates, format and fees. raps.org
Event details are published by the organizer and can change. Confirm dates, format and pricing with RAPS before registering. Verified via WebSearch corroboration, single-primary-source (direct organizer-page fetch was blocked this session) — last checked 21 September 2026.
