Health products policy and standards
Our team provides authoritative guidance and standards on quality, safety and efficacy of health products and supports countries to formulate evidence-based policies and ensure good practice throughout the value chain.

Technical standards and specifications

The WHO normative and standards setting work in the area of medicines, biologicals, blood and other products of human origin has served Member States for 75 years since the establishment of the WHO Constitution.

Biological and pharmaceutical standards

WHO issues international standards and guidance as adopted by Expert Committees.  These norms and standards are important for facilitating production and registration of medicines; establishing the basis for the WHO prequalification process; promoting competition of generics and biosimilars; and contributing to the availability and affordability of quality medicines.

Blood and products of human origin

WHO develops norms, standards, technical guidance and high-level strategic recommendations and provides scientific assessment of current and emerging threats on ensuring availability, safety and quality of blood products and works to improve global access to transplantation of human organs and tissues. The work supports strengthening of country and regional capacity for the supply of quality-assured safe blood products and transplant services improving access to these life-saving treatments.

 

Events

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Publications

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Guidance on implementing patient blood management to improve global blood health status

Incorporating expertise from peers working in countries where health care faces extreme resource constraints, attention  is paid to how PBM processes...

WHO Expert Committee on Specifications for Pharmaceutical Preparations: fifty-eight report

The Expert Committee on Specifications for Pharmaceutical Preparations works towards clear, independent and practical standards and guidelines for...

Implementing cross-border transfer of domestic plasma to obtain plasma-derived medicinal products: policy guidance

The document provides recommendations on legal, regulatory and policy conditions for assuring the quality of plasma for fractionation and protecting the...

Quality assurance of pharmaceuticals: a compendium of guidelines and related materials: volume 1: Good practices and related regulatory guidance, 10th ed

This publication represents a significant achievement in our ongoing effort to ensure that everyone can reach the highest possible level of health. Over...

TRS 1052 - 57th report of the WHO Expert Committee on Specifications for Pharmaceutical Preparations

The Expert Committee on Specifications for Pharmaceutical Preparations works towards clear, independent and practical standards and guidelines for the...

Quality assurance of pharmaceuticals: a compendium of guidelines and related materials: volume 2: Good manufacturing practices and inspection, 10th ed

This publication guides the manufacturing and quality control of pharmaceuticals, vaccines and other biologicals, and other medical products...

Documents

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