The Periodic Safety Update Report (PSUR) & Vigilance under the MDR

This webinar will focus on medical devices with ancillary medicinal substance and the conformity assessment process and key requirements.

In this webinar:

Relevant information you need to know about for the Periodic Safety Update Report.
What information should be presented and how it should be presented.
Understand what types of events are reportable under the Medical Device Regulations (MDR).
Better understanding of the post market requirements as listed under Articles 86 and 87 of the MDR.

Speakers

Speaker

Head of Clinical Compliance, BSI

ติดต่อเรา

ติดต่อเราเพื่อดูว่าเราจะสามารถช่วยแนะนำคุณบนเส้นทางสู่ความสำเร็จในการดำเนินงานอย่างยั่งยืนได้อย่างไร