05 Nov

WHO regards trial registration as the publication of an internationally-agreed set of information about the design, conduct and administration of clinical trials. These details are published on a publicly-accessible website managed by a registry conforming to WHO standards.

What is the ICTRP?

The ICTRP is a global initiative that aims to make information about all clinical trials involving humans publicly available. It also aims to:

  • To improve the comprehensiveness, completeness and accuracy of registered clinical trial data
  • To communicate and raise awareness of the need to register clinical trials
  • To ensure the accessibility of registered data
  • To build capacity for clinical trial registration
  • To encourage the utilization of registered data
  • To ensure the sustainability of the ICTRP

Source: WHO

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