Regulation and Prequalification
Progress towards enhancing regulatory practices related to medical products around the world is supported by capacity building, promoting regulatory convergence and harmonization.

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WHO Drug Information - Volume 38, No. 2

The second issue of Volume 38, includesInternational Nonproprietary Names (INN) Proposed List No. 131

World Local Production Forum on enhancing access to medicines and other health technologies: report of the second meeting, The Hague, Netherlands (‎Kingdom of the)‎, 6–8 November 2023

This report provides an overview of the second WLPF, held from November 6 to 8, 2023, in The Hague, Netherlands (Kingdom of the). Organized by the WHO...

Establishing quality specifications for medicines, vaccines and in vitro diagnostics: week of quality 2023 training kit

Ensuring quality of the health product ensures its safety and efficacy. Manufacturers in low- and middle-income countries (LMICs) face challenges to achieve...

WHO Drug Information - Volume 38, No. 1

The first issue of Volume 38, includesConsultation Documents:fluodeoxyglucose (18F) injection (fluodeoxyglucosi (18F) solution injectabilis)ATC/DDD ClassificationATC/DDD...

Related documents

External assessment report on programmes in the Department of Regulation and Prequalification

External Assessment Report on programmes in the Department of Regulation of Medicines and other Health Technologies

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Report of the meeting of 
the WHO Global Advisory 
Committee on Vaccine 
Safety and the WHO 
Advisory Committee on 
Safety of Medicinal, 
13–15 November 2023

The Global Advisory Committee on Vaccine Safety (GACVS) was established in 1999, and the Advisory Committee on Safety of Medicinal Products (ACSoMP)...

Report of the Meeting of the WHO Global Advisory Committee on Vaccine Safety (GACVS), 15–17 May 2024

The Global Advisory Committee on Vaccine Safety (GACVS) was established in 1999 as an independent expert advisory body to WHO on policies and issues...