Biologicals - World Health Organization (WHO)
Nov 3, 2025 · Biologicals are a class of medicines made from living cells taken from plants, animals or bacteria. These cells are use in creating many types of health care products, …
Good manufacturing practices (GMP) for biological products were first published by WHO in 1992 (1). This current revision reflects subsequent developments that have taken place in science …
Introduction Following implementation of these WHO good manufacturing practices (GMP) guidelines (1) within the context of the WHO Prequalifi cation of Medicines Programme, …
1.2 Transfer of technology is defi ned as “a logical procedure that controls the transfer of any process together with its documentation and professional expertise between development and …
Background The World Health Organization (WHO) published the first edition of the WHO Guidelines on good manufacturing practices for heating, ventilation and air-conditioning …
International Clinical Trials Registry Platform (ICTRP)
The mission of the WHO International Clinical Trials Registry Platform is to ensure that a complete view of research is accessible to all those involved in health care decision making. This will …
General requirements for the sterility of biological substances, …
Requirements for Biological subtances no 6, Revised 1973, Ammendment 1995
Immunization, Vaccines and Biologicals - World Health …
The Immunization, Vaccines and Biologicals department is responsible for targeting vaccine-preventable diseases, guiding immunization research and establishing immunization policy.
mRNA Technology Transfer (mRNA TT) Programme
The mRNA Technology Transfer (mRNA TT) Programme aims to build sustainable regional production of mRNA-based health products, preparing for future pandemics and ensuring …
Health products policy and standards
INNs have been assigned to biological products since the early days of the INN Programme. As well as many names for individual substances, animal insulin preparations were given an INN …