This list contains TCu380A IUD manufacturing sites that have been found to meet the requirements of the TCu380A Intrauterine Contraceptive Device (IUD) WHO/UNFPA Technical Specification and Prequalification Guidance, 2016.

This list contains Female Condom products that have been found to meet the requirements of the WHO/UNFPA Female Condom: Female Condom: Generic Specification, Prequalification and Guidelines for Procurement, 2012.

The following procedure may be used to conduct a remote inspection of male condom manufacturing facilities as part of the WHO/UNFPA prequalification programme.

This form should be completed to request an order through UNFPA for emergency reproductive health kits.

This form should be completed to request an order through UNFPA Procurement Services.

Terms and conditions regarding re-packaging and overbranding activities with not-for-profit finished pharmaceutical products.

This guide is produced for clients utilizing UNFPA’s procurement services for orders projects that require customization of artwork and/or printing on product packaging.

The World Bank’s Borrowers shall use this Standard Form of Agreement when the requirements of the applicable Bank rules for procurement from UN Agencies are satisfied.

To prevent an interrupted supply of the medicines that are under the WHO Prequalification Programme, an interim process called the Expert Review Panel (ERP) is available when less than three prequalified products are offered. The ERP is for those manufacturers that are on their way to prequalification but have not yet achieved this status. UNFPA may allow procurement provided a Notification Form has been completed by the requester and approved by the Quality Assurance Team.