Date: 1st of February (1) and 8th of February (2) 2024 (2 sessions)
Time: 14:00h - 17:00h CET | 9am - 12pm EST
Location: Virtual
Language: English
Costs: € 895,- / $990
The certificate is optional, and will cost an additional € 375,- / $425
Introduction
The MDR and IVDR require that manufacturers and authorized representatives have a person responsible for regulatory compliance. Article 15 of the MDR/IVDR determines the expertise and responsibilities. These have been further clarified in the recent guidance MDCG 2019-07. Qserve organizes training for persons that will be appointed by manufacturers or authorized representatives as PRRC.There is an option to receive a certificate for this training, showing you have successfully qualified as PRRC. The certificate will detail the learning objectives, and if you fulfill the requirements of the MDR/IVDR for qualifying as PRRC (experience and background). The certificate is personalized and can be shown to Notified Bodies during audits.
Learning objectives
- Understand the background of MDR/IVDR to understand PRRC requirements and where they are coming from
- What are the roles and responsibilities of PRRC
- Qualifications of PRRC
- Relation of PRRC and your QMS
- Learn how to appropriately check the conformity of the devices
- Understand what checks are proportionate to the risk class and the type of device
- How to keep the technical documentation and the EU declaration of conformity up-to-date
- Checks to fulfill for post-market surveillance obligations
- Reporting obligations for recording and reporting of incidents and field safety corrective actions
- What to do as PRRC if there are devices undergoing clinical investigation (MDR) or performance studies (IVDR)
- Liability of the PRRC
Who should attend?
- Persons that will be responsible for regulatory compliance
- Authorized representatives
- RA manager, RA director, QA manager, QA director
- Professionals preparing for the MDR/IVDR
Trainer: