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21 reviews for
PRRC Training (Person Responsible for Regulatory Compliance)
12 May 2026 | 1-Day Live Online Course
Original price was: €685.€548Current price is: €548.
Fully understand the PRRC role: Qualifications, responsibilities, task analysis and liabilities
Learn more about the course by toggling through the tabs below.
Course Overview
The Person Responsible for Regulatory Compliance (PRRC) role was created under article 15 of the Medical Device Regulation (MDR) and In Vitro Diagnostics Regulation (IVDR). However, the exact details of the role such as qualifications required, tasks, liability and administrative elements have been unclear for many.
Led by Anne Jury of Team-PRRC, this course will provide you with clarity on the role and all its responsibilities, so your organisation is compliant. You will examine key topics such as qualifications, appointment, registration, tasks, compliance and admin. It is designed for professionals who are a PRRC or considering becoming a PRRC for their organisation. It is also beneficial for management to attend so they fully understand the role of the PRRC.
Key Learning Objectives
- Review the regulation and understand why the role was set up as part of the MDR
- Examine the qualifications required to be a PRRC and how to document this
- Discuss the important elements of appointing a PRRC such as having an agreement / job description
- Registration of the PRRC under Eudamed
- Review the responsibilities of a PRRC of a manufacturer and Authorised Representative and analyse the tasks needed to perform these responsibilities
- Discuss the liability of the PRRC – what does this mean for me?
- In groups examine real-life scenarios to fully cement the course learnings
Who Should Attend?
This course is designed for professionals who are currently a PRRC or looking to take on the responsibility of PRRC in the Medical Device and IVD industry. It also applicable to senior management who would like to get to grips with the role.
Course Information
Course Information
- The course begins at the time stated below
- The course is broken up into sessions outlined below
- There will be breaks between sessions
12 May 2026 | 15 October 2026
1-Day Live Online Training
Register at the top of the page.
Session 1
180 mins | 9:30 AM UK
Introductory overview of MDR 2017/745
- Context of the Person Responsible for Regulatory Compliance (PRRC) according to Article 15 MDR / IVDR and associated recitals
- Comparison with similar roles in other regulations / History of PRRC
Qualifications for the PRRC
- Required qualifications
- Documentation on the responsible person – proof of qualification and competences
Appointment of PRRC
- Job description – scope / duties
- Importance of agreement / contract
- Location of PRRC
Registration of the responsible person
- Eudamed – where and what to register
- Practical implications for PRRC
Tasks of the PRRC
- For PRRC of a manufacturer
- Verification of product conformity, technical documentation, vigilance activities, post-marketing surveillance (PMS), compliance of investigational or performance evaluation devices with Annex I
- For PRRC of an authorised representative (AR)
- Ensuring compliance with the mandate between AR and Manufacturer
Session 2
180 mins | 1:30 PM UK
Choosing the appropriate practical working methods to demonstrate compliance
- Reports
- Audits
- Spot checks
- Review and approval of relevant procedures/ forms / documents
- Inclusion of PRRC responsibilities within the QMS
Administrative considerations
- Availability
- Liability
- Implications of the special provision for micro, small and medium-sized enterprises I.e. dealing with the external PRRC
Aptitudes required for successful PRRCs
- Ensuring the PRRC has the organisational freedom to operate effectively (from both employer and PRRC perspective)
- Interdepartmental and interpersonal communication requirements
- Dealing with difficult situations
Workshop
Work through a real-life scenario, tasks required, methods to use, consequent actions and results.
Anne Jury is a consultant and trainer in medical devices EU & UK regulatory compliance and quality assurance systems. Starting out as company microbiologist for Smith & Nephew Textiles Anne went on to work for Notified Bodies, BSI and then TÜV Product Service as a lead auditor and later as UK Regional Manager.
Anne has run her own consultancy business since 2000 providing medical device regulatory support to companies ranging from research institutes and start-up companies to SMEs and multi-national market leaders. Anne was one of the founders and visiting lecturers to the MSc in Medical Technology Regulatory Affairs run by TOPRA and Cranfield University where she was also external examiner from 2009 to 2012.
Anne has extensive MDR expertise, supporting her clients transition from the MDD as new guidelines and ISO standards are published. As a result, she can draw on multiple case study examples and experience when delivering MDR training courses. Anne has led both in-house and public courses on medical device EU regulatory affairs for several years.
Anne is also Vice-President of Team-PRRC, a non-profit organization set up in March 2020 to support individuals in the role of PRRC under the EU medical device regulations.
Format, Dates & Times
Find out when this course is running so you can plan your training. Scroll down to view the full agenda.
12 May 2026
1-Day Live Online Training
Register at the top of the page.
15 October 2026
1-Day Live Online Training
Register at the top of the page.
On-Demand Access
Can’t wait for the next course date?
Get instant access to the training materials by selecting ‘On-Demand’ from the drop-down menu above. Start learning at your convenience. You’ll also be added to the next live session, giving you the opportunity to attend and interact directly with the trainer if you wish.
Course Times
For live online delivery, the course starts at 9:30 AM (UK time) and finishes at 4:30 PM (UK time).
Group Discount
If you want to train a small group, we offer a group discount between 5% and 50% depending on the course and number of attendees.
For a quote, complete our contact form by following the link. Get in touch.
Customised Team Training
We also design and deliver fully customised team training focused on your products, processes, technologies and challenges. This is ideal for specific training requirements or larger groups. Please get in touch with us for more information.
For more information, complete our contact form by following the link. Get in touch.
What is Included?
Certification
Download your official Educo Life Sciences Certificate of Attendance to showcase your achievement and professional development.
Access to Recordings for 2 Weeks
Enjoy unlimited access to all session recordings for up to two weeks after the final session — perfect for revision or catching up.
Learner Reference Guide
Attendees receive an overview packed with key concepts, examples, and references from your training to support you long after the course concludes.
On-Demand or Live Online
This course is delivered live or you can access on-demand materials immediately to begin learning straight away.
6 Hours of Learning
This course includes a total of 6 hours of learning.
Expert Trainer
Engage directly with leading trainers who bring real-world experience and insider knowledge to every session.
Additional Course Information
Free Online Module
Free Online Module
- Some of our courses include a free to attend module 1. Please check above to see if this applies to this course.
- If applicable, module 1 is free to attend and delivered online at a date 3 to 8 weeks before the full course start date.
- To register for module 1, please submit your details in the form located above.
- Module 1 is recorded so if you are unable to attend, you can catch up ahead of the course start date.
Full Course Information and Pricing
Full Course Information and Pricing
- To attend the full course, you must register online at the top of the page by selecting the course dates from the drop-down and clicking enrol to add the course to your basket. Once added, please follow the checkout instructions to pay via credit card or bank transfer.
- There are price tiers for this course. The dates of these are located above. The earlier you register the more you save.
- The full training course is delivered either online or in a classroom. Please check which course format you have booked.
- For hybrid training – In the event we do not have enough people on one of the options we will contact you to discuss switching.
- For live online courses – The dates and times of modules/sessions are subject to change.
- For live online courses – The module/session durations are approximate.
On-Demand Information and Pricing
On-Demand Information
- Most courses are available on-demand. If you select this option you will be able to begin training instantly.
- You will gain access to a previous live online session, slides and learner reference guide.
- You will also be added to the next live session, giving you the opportunity to attend and interact directly with the trainer if you wish.
- Depending on the course length you will have access to the on-demand materials for 1 to 3 months.
21 reviews for PRRC Training (Person Responsible for Regulatory Compliance)
12 May 2026 | 1-Day Live Online Course
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SIA Latvia MGI Tech –
Well organized, trainer was so energetic. Majority of the content will be very useful in my daily work. Hope to attend other training courses too.
Skin Tech Pharma Group –
The course was really interesting and updated. It gives you a clear vision on the requirements and responsabilities of the position.
Biokit S.A. –
Complete and clear course on the PRRC role & responsibilities, with numerous and insightful collaborative discussions with speaker and attendees.
Skin Tech Pharma Group –
All good, very satisfied.
Skin Tech Pharma Group –
Very good experience. The trainer is a high-level expert.
SIA Latvia MGI Tech –
All good, satisfied
Reckitt Benckiser –
I’m new to this area and the opportunity to have a really in depth view, with lots of questions and discussion was fantastic.
Reckitt Benckiser (verified owner) –
Very beneficial in understanding the requirements on a deeper level and practical considerations.
Purple Surgical Manufacturing Ltd –
Excellent course, well presented and great to hear ideas from a range of different companies and how they approach different situations.
Reckitt Benckiser (verified owner) –
This course was very insightful and the use of real life examples really made you think. The course was very interactive and would definitely recommend to other companies if this is an area of interest for them
ANT Neuro B.V –
The requirements in Art. 15 and the guidance MDCG 2019-7 were further elaborated. The first-half of the course will help somebody who has no information on this. For people who have already read and understood the requirements, the second-half of the course might provide more insight with the quizzes and exercises.
RR Mechatronics Manufacturing B.V. –
Very informative, good trainer and enough information to find out what the Role of PRRC contains.
Owlpharma Consulting, Lda. (verified owner) –
The presenter Anne Jury was very nice, knowledgeable and provided a very interactive session. Loads of topics were mentioned, information that I could not access just by reading the regulation. definitely useful.
ResMed –
Very informative session where it was presented in an easy to understand manner.
MDR Regulator Sp. z o.o. (verified owner) –
Very well organised training. Professional trainer, great prepared materials. Highly recommended!
BioTop Medical (verified owner) –
Very good course, informative and well-structured. I learned a lot which I can certainly apply in my future role as PRRC.
ExamenLab Ltd –
Great course. Found it very useful!
Shelley Quality Management Services Ltd (verified owner) –
The Educo PRRC course was perfect for both sub-contract PRRCs and in house ones, for both manufacturers and distributors/importers. The delivery, of what can be quite dry regulatory requirements, was perfectly pitched with great worked examples, and there were plenty of opportunities to delve deeper and debate interpretation. A great course providing the training required to demonstrate as a PRRC that the person is suitably trained and qualified to carry out the role.
Eurodrug Laboratories B.V. (verified owner) –
Great course, very pragmatic and informative
Sterimedix (verified owner) –
I would highly recommend this course. I found it very informative and enjoyable.
Sterimedix –
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