Medical Device Risk Management and Quality Systems: ISO 14971 and ISO 13485 – Paris, 23–27 Aug 2027
Medical Device Risk Management and Quality Systems: ISO 14971 and ISO 13485 runs in Paris from Monday 23 August to Friday 27 August 2027 (1 Week). The fee is 23,500 SAR per participant. The same programme is also scheduled in 7 other cities.
- Dates
- Length
- 1 Week
- Fee per participant
- 23,500 SAR
- Format
- In person, Paris
- Venue
- Right Bank business hotel
- Status
- Open for registration
- Week
- 34 of 2027
- Reference
- 265_11776
This session
23–27 Aug 2027
This Medical Device Risk Management and Quality Systems: ISO 14971 and ISO 13485 session in Paris runs from Monday 23 August to Friday 27 August 2027 (week 34, Q3 2027). It is the 2nd of 2 dates in Paris in 2027, at a fee of 23,500 SAR, the same for each of them. Registration is open for this date. It is held in person at Right Bank business hotel.
When else does it run in Paris?
- 15 – 19 March 2027 23,500 SAR
- 23 – 27 August 2027 This date 23,500 SAR
How do I book this date?
Register online to request your place, or send us a question about this date first.
Reference for this date: 265_11776. Quote it when you contact us.
Before you book, read our cancellation policy.
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Questions about this date
When does Medical Device Risk Management and Quality Systems: ISO 14971 and ISO 13485 in Paris start and finish?
It starts on Monday 23 August and finishes on Friday 27 August 2027: 1 Week.
How much does Medical Device Risk Management and Quality Systems: ISO 14971 and ISO 13485 in Paris cost?
The fee for this date is 23,500 SAR per participant. Please read our cancellation policy before you book.
Is this date held in person or online?
It is held in person in Paris, at Right Bank business hotel.
What does this programme cover?
Medical device risk management fails when hazards are listed once at design stage and never revisited, when quality records cannot show why a residual risk was accepted, and when complaints and field reports never reach the risk file. This Core Concept course takes manufacturers, distributors and hospital biomedical teams through device classification, an ISO 13485 quality management system and the ISO 14971 process: hazard identification, risk estimation and evaluation, risk controls, benefit-risk decisions and post-production information. Participants build a Device Risk Management File for a product from their own work.
The programme outline covers:
- Introduction
- Course Objectives
- Target Audience
- Course Outline
- Day 1: Medical Device Fundamentals, Classification and Current-State Review
- Day 2: ISO 13485 Quality Management System for Devices
- Day 3: ISO 14971 Risk Management Process Application
- Day 4: Risk Controls, Benefit-Risk, Usability, Software and Post-Market Feedback
- Day 5: Case Study Workshop: Device Risk Management File
- Skills You Will Gain
- Why Attend This Course
- Conclusion
Where else does this programme run?
Also scheduled in 7 other cities.
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