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
Average rating 4.6
I felt the course was very interactive, intimate (not too many delegates) and it was the correct duration for the course.
The detailed content was broken down into bitesize chunks. The course was engaging and covered a variety of topics.
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.
The cost of this training course is £1595 + VAT per participant, which covers tuition and course materials.
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.