This webinar session answers your most-asked questions about safety and performance objectives, clinical outcomes, clinical benefits, acceptance criteria, and risk-benefit ratio. We hope to provide you with best practices and writing strategies to support solid planning during your own writing process.
Who is this webinar for?
Those Regulatory, Quality and Clinical leaders and teams who are tasked with the development, writing, review, or approval of clinical evaluation reports for MDR submissions or performance evaluation reports for IVDR submissions.
|October 5th, 2022||Watch at a Convenient Time||Recorded|