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Clinical trials - World Health Organization (WHO)
The ICTRP is a global initiative that aims to make information about all clinical trials involving humans publicly available It also aims to: improve the comprehensiveness, completeness and accuracy of registered clinical trial data; communicate and raise awareness of the need to register clinical trials; ensure the accessibility of registered
International Clinical Trials Registry Platform (ICTRP)
For the purposes of registration, a clinical trial is any research study that prospectively assigns human participants or groups of humans to one or more health-related interventions to evaluate the effects on health outcomes Clinical trials may also be referred to as interventional trials
Glossary - World Health Organization (WHO)
Biomedical clinical trials of experimental drug, treatment, device or behavioral intervention may proceed through four phases: Clinical trials test a new biomedical intervention in a small group of people (e g , 20-80) for the first time to evaluate safety (e g , to determine a safe dosage range and to identify side effects)
Guidance for best practices for clinical trials
The Guidance for Best Practices for Clinical Trials has been developed in response to the 2022 World Health Assembly resolution (WHA75 8) on strengthening clinical trials This guidance provides Member States with a framework for integrating robust and ethical clinical trial practices into their national health systems, enhancing the quality
WHO Global Clinical Trials Forum (GCTF) - World Health Organization (WHO)
The network aims to enable activities of partners for implementation of WHO's guidance on best practices for clinical trials, guidance developed at the request of World Health Assembly resolution WHA 75 8 A Global Action Plan for Clinical Trial Ecosystem Strengthening re-articulates the WHO guidance in the form of key actions for implementation
Guidance for best practices for clinical trials
In response to the World Health Assembly resolution (WHA75 8) on Strengthening clinical trials to provide high-quality evidence on health interventions and to improve research quality and coordination, the guidance emphasizes the importance of patient, participant, and community engagement in clinical trials to ensure research aligns with public needs and maintains trust Key recommendations
Chinese Clinical Trial Registry (ChiCTR) - World Health Organization (WHO)
10 Is the WHO Trial Registration Data Set electronically searchable? (ICMJE) Yes 11 Is the WHO Trial Registration Data Set available in English? Yes 12 Can registrants submit a trial for registration at any time of day on any day of the week (24 hours a day, seven days a week)? Yes 13
A starting point, not an endpoint: WHOs new clinical trials guidance . . .
In September 2024, the World Health Organization (WHO) launched its landmark publication "Guidance for best practices for clinical trials" This pivotal document is described as "not an endpoint but a starting point" (1) for enhancing global health through robust, ethical, and inclusive clinical research It serves as a foundational resource aimed at improving the design, conduct, and
Public consultation on WHO guidance for best practices for clinical trials
Important stakeholder groups for this technical guidance include, (but are not restricted to): public sector researchers, private sector entities engaged in clinical trials, national health authorities or research councils involved in health research, clinical trial registries, research ethics bodies, national or transnational medicinal product