WHO Expert Committee on Pharmaceutical Preparations Meeting
Summary
The World Health Organization (WHO) announced the Sixtieth meeting of the Expert Committee on Specifications for Pharmaceutical Preparations, scheduled for October 12-16, 2026. This committee advises the Director-General on medicine quality assurance and the maintenance of The International Pharmacopoeia.
What changed
The World Health Organization (WHO) has announced the upcoming Sixtieth meeting of the Expert Committee on Specifications for Pharmaceutical Preparations, to be held from October 12-16, 2026, at WHO headquarters in Geneva. This committee plays a crucial role in advising the Director-General on the quality assurance of medicines, overseeing The International Pharmacopoeia, and providing guidance to regulatory authorities in Member States to ensure medicines meet unified standards of quality, safety, and efficacy. The committee also recommends regulatory guidelines for multisource medicines intended for global use.
This meeting is primarily informational, serving as a platform for discussion and recommendation regarding pharmaceutical quality standards. While it does not impose immediate compliance obligations or deadlines on regulated entities, it informs the development of future guidelines and standards that pharmaceutical manufacturers and regulatory authorities worldwide will need to adhere to. Compliance officers should note the committee's role in shaping international pharmacopoeial standards and regulatory guidelines.
Source document (simplified)
WHO / Christopher Black
WHO headquarters in Geneva, Switzerland. Statue commemorating the 30th anniversary of the eradication of smallpox. © Credits
Sixtieth meeting of the WHO Expert Committee on Specifications for Pharmaceutical Preparations
12 – 16 October 2026
The Expert Committee on Specifications for Pharmaceutical Preparations advises the Director-General on quality assurance of medicines. It oversees the maintenance of The International Pharmacopoeia and provides guidance for use by relevant WHO programmes and regulatory authorities in Member States, to ensure that medicines meet unified standards of quality, safety and efficacy. The Committee recommends regulatory guidelines of importance to multisource medicines designed to be used globally.
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