Date & Time: Wednesday 15 March, 1.00-2.00 PM CET
Participants: Manufacturers of prequalified IVDs
Aim / Goal: The aim of this workshop is to provide in vitro diagnostics (IVDs) manufacturers with prequalified products an update on the implementation of the Collaborative Registration Procedure (CRP).
Learning objectives: participants will learn about:
- The principles and objectives of the CRP
- The process for participation
- The countries currently engaged with the CRP for IVDs
- Up-coming plans for supporting CRP implementation
Format: The Zoom video conferencing platform will be used. The workshop will include presentations by key staff from the WHO Regulation and Prequalification department. The Q & A session will address questions raised during the workshop using the chat function.
Participants can register in advance for the Zoom session using the link: https://who.zoom.us/webinar/register/WN_s9Hxc6HiSsu9gPDNdb2lHA
Target audience: The information session is suitable for IVD manufacturers with products that are prequalified or that are currently undergoing prequalification assessment.
| Time | Topic | Facilitator |
|---|---|---|
| 5 mn | Welcome and opening remarks | Irena Prat |
| 15 mn | PQ Assessment and CRP reports | Susie Braniff |
| 15 mn | Updates on the Collaborative Registration Procedure | Agnes Kijo |
| 20 mn | Poll + Question & Answer session | Susie Braniff |
| 5 mn | Wrap-up and close | Irena Prat |