TRS 1060 - Annex 8: Collaborative registration procedure between WHO and national regulatory authorities in the assessment and accelerated national registration of WHO-prequalified vector control products

The CRP is applicable to VCPs that have been assessed by the WHO Prequalification Unit in line with the procedures and standards available at the WHO website page on vector control products (4) and that have been found to be acceptable in principle for procurement by United Nations agencies and WHO Member States, as listed in the WHO List of Prequalified Vector Control Products (5). 

The CRP serves to accelerate the assessment and registration of VCPs prequalified by WHO. It covers national registration and management of product life cycle activities (for example, variations, post-approval changes, delisting, deregistration or withdrawal).