Скачать или смотреть Squash Software Issues in Your EU MDR Technical Documentation Review 20251029

Are you a manufacturer currently leveraging the extended timeline for EU MDR 2017/745 compliance? Benefit from important lessons we’ve learned from our work with SaMD technical documentation review.

ARE YOU READY?
Join industry experts from ELIQUENT Life Sciences' and Notified Body Scarlet for a free, must-attend webinar where we’ll provide actionable insights, practical recommendations, and implementation strategies to help you navigate EU MDR implementation for software as a medical device with confidence.


–What You’ll Learn–
During this insightful webinar, Scarlet Notified Body’s Head of Devices, Dr. Sandy Wright, and ELIQUENT experts Kimberly McCoy and Michael Dunn will break down these essential topics:


☑️ Common pitfalls with technical documentation (TD) submissions

☑️ Notified Body perspective on software as a medical device (SaMD) submission to EU MDR – what works and what doesn’t

☑️ How to create a compliant risk management process connected with post-market surveillance (PMS) and clinical evaluation reporting (CER)