Post-market Surveillance under MDR & IVDR Virtual Training

Post-market Surveillance & Vigilance under Medical Device Regulation & In Vitro Diagnostics Medical Devices Regulation Virtual Training

Post-market Surveillance under MDR & IVDR Virtual Training

Level Implementation Duration 1 days

Available to book: Live online classroom View dates and book now

BSI’s ‘Post-market Surveillance and Vigilance under the Medical Device Regulation (MDR) and In Vitro Diagnostics Medical Devices Regulation (IVDR)’ one-day training course has been designed to provide manufacturers with the tools to implement an appropriate system for gaining and reviewing experience in the post production phase from the range of devices they manufacture.

How will I benefit?

The course will help you:

Understand the key requirements and concepts of the post-market surveillance and vigilance for the MDR and IVDR
Gain sufficient understanding to be able to write your PMS and vigilance procedures
Communicate the impact of these key requirements introduced by the MDR and IVDR to your organization
To obtain essential knowledge to implement a compliant post-market surveillance and vigilance quality management system
To understand how the PMS and vigilance processes integrate into the quality management system

On completion of this training, you’ll be able to:
- Interpret regulatory requirements for post-market surveillance and vigilance under the MDR and IVDR
- Identify how these requirements relate to ISO 13485:2016, ISO 14971:2019 and various European and IMDRF (GHTF) guidance documents
- Create a post-market surveillance plan that includes both proactive and reactive sources of information
- Implement appropriate post-market clinical follow-up (PMCF) and post-market performance follow-up (PMPF) as per the MDR and IVDR respectively
- Recognize when incidents and adverse event need to be reported to the Competent Authorities and Notified Bodies for both pre and post CE marked devices
This course is ideal for you if you’re in a quality assurance/quality control/regulatory/patient safety/customer facing role involved in continuous improvement and customer advocacy.
On completion, you’ll be awarded an internationally recognized BSI Training Academy certificate.
If you have any enquiries, let us know how can we help you.
Call: +91 80815 80815
Email us: info.in@bsigroup.com
"This training fee is applicable only for residents of India and the Indian subcontinent"
- This training content will be delivered via BSI’s Connected Learning Live Platform as a virtual classroom with the BSI tutor. This will provide the delegate with the flexibility of attending it from the convenience of home or office, without travelling to BSI facility. A stable internet connection, headset with USB connection, a quiet and suitable work area. In advance of the training a ‘testing room’ will be provided for delegates to confirm their hardware works and that they can fully participate in the training.
- Examination will be conducted online via an e-assessment platform 'Questionmark'. Invigilation will be done through delegate’s webcam and microphone.
  
  Please Note: This training fee is applicable only for residents of India and the Indian subcontinent.

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