NSF has announced it will be hosting a complimentary webinar that will discuss the requirements of Regulation 2017/746 (IVDR) on performance evaluations.
Visitors can learn about the three cornerstones of performance evaluation: scientific validity, analytical performance and clinical performance.
The company will present its preliminary template for writing performance evaluation reports. You can obtain the unique opportunity to get first practical implementation concepts on how to write performance evaluation reports according to Annex XIII of Regulation 2017/746.
This webinar will be presented by NSF’s in-vitro device (IVD) expert Janina Rumker, who will provide deep insight into medical writing.
Prepare for the future and learn how to plan, continuously conduct and document a performance evaluation.
About the presenter
Janina Rumker is the senior consultant and quality management representative at PROSYSTEM. With several years of professional experience in the field of regulatory and clinical affairs, she is an expert in the implementation of European regulatory requirements, especially with regard to the new IVD Medical Device Regulation 2017/746.
She holds a Bachelor’s Degree in Biomedical Engineering Science and a Master of Business Administration.
If you are interested in attending this webinar, please make an enquiry using the form on this page.