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Advanced Regulatory Affairs for Medical Devices

Course summary
2 days
1,595 GBP excl. VAT
Berlin, Brussels, City of London
Next available date: 23/09/2020 - Brussels
Professional Training

Course description

Advanced Regulatory Affairs for Medical Devices

Advanced Regulatory Affairs for Medical Devices - A Pharma Training Course by PTI

The Medical Devices Regulation (MDR) was concluded in June 2016, which means significant changes for the European regulatory landscape for medical devices. This course will ensure that participants are completely up-to-speed with the latest regulatory updates and will equip them with the knowledge and confidence to develop optimal regulatory strategies, ensuring compliance during this period of change.

Suitability - Who should attend?

This training programme is aimed at professionals specialising in Medical Device operations within the pharma industry.

Training Course Content

Training course content will cover:

  • The NEW Medical Devices Regulation (MDR)
  • Strategies to implement the new MDR 
  • Changes to roles and responsibilities of key stakeholders
  • Advanced tools needed to optimise and maintain regulatory procedures
  • Common problems and solutions

Why choose PTI

On average, delegates of their online academies said: 

Quality of content:


85% had applied content during the course to their role

Delivery rating:



The cost of this training course is £1595 + VAT per participant, which covers tuition and course materials.

In-house Training

PTI - Pharmaceutical Training International can also deliver this course as in-house training for your company. You can reduce costs, enhance accessibility to training resources and better address your company’s own business goals with a tailored PTI training package.

About provider

PTI - Pharmaceutical Training International

PTI - Pharmaceutical Training International - Training for the Pharma Industry

PTI is the global leader in professional education for the pharmaceutical industry, delivering a broad course portfolio that covers the industry spectrum: R&D, Clinical Development, Generics, Bio-pharmaceuticals, fine Chemicals, Agro-chemicals, Medical Devices, Animal Health, Manufacturing and Regulations. PTI's open courses,...

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Average rating 4.6

Based on 5 reviews

Technical Manager, JensonR+ Limited
I felt the course was very interactive, intimate (not too many delegates) and it was the correct duration for the course.
Senior Regulatory Affairs Specialist (EMEA & Canada), HOLOGIC LTD
The detailed content was broken down into bitesize chunks. The course was engaging and covered a variety of topics.
Head of Project Management, Team Consulting
There was a small class and it had really good detailed sessions. I took this course to gain an understanding of the old vs new MDR.
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Course rating
Based on 5 reviews
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