An online information session about the Prequalification of glucose monitoring devices was held for manufacturers on Friday 5 November.

The 9th annual collaborative registration procedure (CRP) meeting for National Regulatory Authorities (NRAs) was held 13 - 17 December.

The In Vitro Diagnostics Assessment Team continues its focus on assessing IVDs for detection of SARS-CoV-2 under the WHO Emergency Use Listing assessment procedure.