Quality & Productivity

Medical Device Risk Management and Quality Systems: ISO 14971 and ISO 13485 – Dubai, 3–7 May 2027

Medical Device Risk Management and Quality Systems: ISO 14971 and ISO 13485 runs in Dubai from Monday 3 May to Friday 7 May 2027 (1 Week). The fee is 19,500 SAR per participant. The same programme is also scheduled in 7 other cities.

Dates: Monday 3 May – Friday 7 May 2027
Length: 1 Week
Fee per participant: 19,500 SAR
Format: In person, Dubai
Venue: Five-star CBD venue
Status: Open for registration
Week: 18 of 2027
Reference: 265_11771

This session

3–7 May 2027

This Medical Device Risk Management and Quality Systems: ISO 14971 and ISO 13485 session in Dubai runs from Monday 3 May to Friday 7 May 2027 (week 18, Q2 2027). It is the 2nd of 2 dates in Dubai in 2027, at a fee of 19,500 SAR, the same for each of them. Registration is open for this date. It is held in person at Five-star CBD venue.

When else does it run in Dubai?

1 – 5 March 2027 19,500 SAR
3 – 7 May 2027 This date 19,500 SAR

How do I book this date?

Reference for this date: 265_11771. Quote it when you contact us.

Before you book, read our cancellation policy.

Let’s talk about your next step.

Questions about this date

When does Medical Device Risk Management and Quality Systems: ISO 14971 and ISO 13485 in Dubai start and finish?

It starts on Monday 3 May and finishes on Friday 7 May 2027: 1 Week.

How much does Medical Device Risk Management and Quality Systems: ISO 14971 and ISO 13485 in Dubai cost?

The fee for this date is 19,500 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 Dubai, at Five-star CBD venue.

Where else does Medical Device Risk Management and Quality Systems: ISO 14971 and ISO 13485 run?

It is also scheduled in 7 other cities: Amsterdam, Barcelona, Dammam, Jeddah, London, Paris and Riyadh.

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