Once an in vitro diagnostic medical device (IVD) or a male circumcision device (MCD) is prequalified, a WHO Prequalification Public Assessment Report (WHOPAR) and a separate Public Inspection Report (WHOPIR) are posted on this website. 

For IVD and MCD products which were prequalified prior to 2025, one WHO Prequalification Public Report contains the outcome of all prequalification assessment components including any inspection of the manufacturing site(s) that manufacture that product.

WHOPIR and WHOPAR are key prequalification outputs, providing insight into prequalification processes and helping to ensure that those processes are transparent. Other key prequalification outputs for IVDs include the WHO List of Prequalified In Vitro Diagnostic Products.