Person Responsible for Regulatory Compliance Course: 2nd – 4th December 2019
The PRRC course is a comprehensive course with the aim of enabling attendees to act as a “Person Responsible for Regulatory Compliance” under the Medical Device and In-Vitro Diagnostic Medical Device Regulations (MDR & IVDR).
During a 3-day course, different industry experts will cover the requirements of the regulations for both medical devices and in-vitro diagnostics and concentrate on those aspects that need to be understood by the PRRC.
Who should attend
The course is open to anyone with an interest and knowledge in the medical device and in-vitro diagnostic industries. The course is suitable for delegates at all levels of knowledge, from beginners to those who are already active in the industry.
The course takes place at Obelis Headquarters: Boulevard Brand Whitlock 30, B-1200 Brussels,Belgium
Clinical Evaluation Reporting Workshop: 30th October 2019, Tel Aviv, Israel
Learn about clinical data management, setting up a literature research and compiling a clinical evaluation report by means of a practical workshop based on different real-life study cases. Subscribe and find out more information here.
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