May 27, 2020 - May 27, 2020
Date: 27th of June 2020
Time: 18:00h - 19:00h CEST / 12.00am - 13.00pm EDT
Trainer: Jasmin Hunter
Clinical Evaluation requirements have increased dramatically since the release of MEDDEV 2.7.1 Rev 4 in 2016 and the MDR 2017/745 in May of 2017. All of these changes require discussion by the cross-functional teams involved in these key roles to minimize duplication of work and ensure consistency across documentation. This free webinar will provide an overview of the types of data required for clinical evaluation from the design control process, clinical investigations, post market surveillance, post market clinical follow-up, and risk management. This information provides a platform to determine the best approach for report delivery timelines and content that will make the clinical evaluation process more efficient.