Medical Device Regulation (EU MDR) 2017/745
Training Methods: Virtual Training ○ On-Site ○ Bespoke ○ eLearning Coming Soon
The MDR (EU 2017/745) has replaced the MDD (93/42/EEC) as the legislation detailing the requirements that manufacturers must comply with in order to place medical devices on the market within the EU.
Our industry leading experts have created a 2-day MDR training course to help medical device manufacturers understand the additional requirements of the regulation, so you know what you need to do for your business and products to meet the new MDR.
The certification you will earn from this training can be used to demonstrate your knowledge to your Employers and Notified Bodies.
At A Glance
- 2-days of fully interactive training
- Instructor-led virtual classroom
- PDF Certificate of completion
- Live Q&A sessions
- Indexed copy of the MDR
- PDF Copies of the slides, handouts and templates
- 15% off the EU MDR Guidebook
- Bespoke and on-site training available
Who Should Attend?
This training course is recommended for anyone making and selling devices into the European Union:
- Regulatory Affairs Professionals
- Research and Design Engineers
- Quality Managers
- Quality Engineers
- Authorised Representatives
"Thank you for providing me with a high level overview of the Medical Device Regulation 2017/745, the course has helped me to understand what I need to do in order to transition the business from the Medical Device Directives (93/42/ECC), I would highly recommend this course."
"Thanks a million, the course was excellent and very enjoyable!"
"I have learnt a lot from this course and it is excellent to get insights and advice from the experts, thank you. I particularly enjoyed the Q&A session"