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Academy: PRRC Workshop Advanced

Medical device —
16 - 18 februar
09:00 - 17:00

Online

This 3-day workshop on Person Responsible for Regulatory Compliance (PRRC) is an advanced training for those who are looking to acquire the knowledge to act as PRRC in their own organizations. Led by experts and leaders in the industry, the course will provide you with in-depth understanding of the technical documentation, essential requirements, classification, conformity assessment, clinical investigation and evaluation and post-market surveillance. In one word, everything that a PRRC should know. Register now!

At the end of this training, you will be able to have an in depth knowledge of the MDR/IVDR requirements, as well as the profession of PRRC.  More specifically, you will learn how to appropriately check the conformity of the devices,  establish verification which are proportionate to the risk class and the type of device, maintain the technical documentation and the EU declaration of conformity up-to-date, proceed with reporting and verify the post-market surveillance obligations.

Who should attend :

  • Medical device manufacturers management
  • Staff that will be responsible for regulatory compliance
  • RA manager, RA director, QA manager, QA director
  • Professionals preparing for the MDR/IVDR

To attend this workshop, you must have completed Beginners workshop (or have relevant experience – to be evaluated by course instructor)

Schedule:

Day 1 10:00 – 10:50 —– Essential requirements – Janette

10:50 – 11:00 —— coffee break

11:00 – 12:00 —– Technical file – Theory – Roland

12:00 – 12:30 ——Technical file – Exercises – Roland

12:30 – 13:30 —– Lunch time

13:30 – 14:30 —— Labelingtheory – John Webster

14:30 – 14:45 —— coffee break

14:45 – 15:45 ——- Labeling –  cases study – John Webster

15:45 – 16:30 —– Panel Q&A – Closing words

 

Day 2 10:00 – 10:45 – Classification – MDR – Theory – Janette

11:00 – 11: 45 Classification –– MDR – Exercises – Janette

11:45 – 12:00 Coffee break

12:00 – 12:45 Classification – IVDR – Theory – Louise

12:45 – 13:45 Lunch break

13:45 – 14:45 Classification – IVDR – Exercises – Louise

14:45 – 15:00 Coffee break

15:00 –15: 45 Conformity assessment – Theory –  Bassil

15:45 – 16:30 Conformity assessmentExercise – Bassil

16:30 – 17:00 Panel Q&A – Closing words

 

Day 3 10:00 – 11:30 Clinical Evaluation – Theory – Louise

11:30 – 12:00 Clinical Evaluation – In practice – Helen

12:00 – 13:00 Lunch break

13:00 – 14:30 Clinical Investigation – Theory – Janette

14:30 – 15:00  Clinical Investigation – In practice – Helen

15:00 – 15:15 Coffee break

15:15 – 16:00 Panel Q&A – Final closing words

Pricing:

  • For Norway Health Tech members: NOK 10 000
  • For members of other clusters and incubators: NOK 11 000
  • For non-members: NOK 14 000

There are limited spaces on the training, so sign up now if you want to secure your spot (and commit to participating).

You can also sign up for information, but you will not have secured a spot. But we will know you are interested in regulatory training and send you information on regulatory training from Norway Health Tech Academy.

If you have any questions, please contact our Regulatory Advisor Kami Faust.

 

 

 

Norway Health Tech Academy is supported by Innovation Norway

Påmelding

Speakers

Kami Faust

Regulatory Advisor - Norway Health Tech

kami.faust@norwayhealthtech.com

Bassil Akra

CEO - QUNIQUE GmbH

bassil.akra@quniquegroup.com

Louise Olliver

Regulatory expert - Obelis

Janette Benaddi

Consultant - https://www.obelis.net/

jbenaddi@outlook.com

Helene Quie

Co-Founder & Senior Advisor - Qmed Academy