Overview

Over the next few weeks we will be adding five insightful webinars to this page, so please stay tuned as new webinars are published.

These five intuitive webinars will help you focus on various aspects of the MDR, from preparing a Clinical Evaluation Plan, to supporting you with preparing a Clinical Evaluation Report, with an in-depth, 2 - part webinar. Additionally, we’ll also give you advice around preparing a Post Market Clinical Follow Up Plan and Evaluation Report (PMCF) as well as helping you to understand how best to produce a compliant SSCP for both healthcare professionals and patients.

Key takeaways and learning objectives

Topics covered in this Session on Post Market Clinical Follow-up:

• SSCP Requirements and Purpose
• SSCP Updates
• SSCP Submissions
• A few Pointers
• Device Groupings
• Link from the IFU to the SSCP

Presenter information

Join Sheila Walsh, Clinical Regulatory Lead at BSI as she talks about preparing Summary of Safety and Clinical Performance (SSCP).