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  • WHO data set
    Secondary Sponsor (s) Additional individuals, organizations or other legal persons, if any, that have agreed with the primary sponsor to take on responsibilities of sponsorship
  • Chinese Clinical Trial Registry (ChiCTR)
    All countries 2 2 If the Registry is not open to ALL registrants (that is, accepts trials only from a particular sponsor, health care condition (eg cancer), intervention, etc) please specify which trials the Registry is open to Not applicable 3 Is the Registry able to collect and publicly display the WHO Trial Registration Data Set? (ICMJE
  • Australian New Zealand Clinical Trials Registry (ANZCTR)
    If the Registry is not open to ALL registrants (that is, accepts trials only from a particular sponsor, health care condition (eg cancer), intervention, etc) please specify which trials the Registry is open to
  • Safety Platform for Emergency vACcines
    The study sponsor constitutes the individual DSMBs and the study DSMB has direct responsibility for oversight of the trial and reports to the sponsor The goal of the Meta-DSMB is to provide overall oversight for all CEPI-funded vaccine clinical trials by identifying potential safety concerns: Across trials using the same platform
  • Clinical Research Information Service (CRiS) of Republic of Korea
    Republic of Korea 2 2 If the Registry is not open to ALL registrants (that is, accepts trials only from a particular sponsor, health care condition (eg cancer), intervention, etc) please specify which trials the Registry is open to Not applicable 3 Is the Registry able to collect and publicly display the WHO Trial Registration Data Set
  • Sponsorship of health professional associations by manufacturers and . . .
    This brief describes how six Health Care Professional Associations (HCPA), in different countries and years, carried out a process that led to an end of their collaboration with companies that market foods for infants and young children as far as sponsorship of HCPA events is concerned
  • 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 improve research transparency and will ultimately strengthen the validity and value of the scientific evidence base The registration of all interventional trials is a scientific, ethical and moral
  • Research Ethics Review Committee
    The Research Ethics Review Committee (ERC) is a 27-member committee established and appointed by the Director-General Its mandate is to ensure WHO only supports research of the highest ethical standards The ERC reviews all research projects, involving human participants supported either financially or technically by WHO While the majority of the committee consists of WHO staff
  • Declaration of Helsinki WorldMedicalAssociationDeclarationofHelsinki
    Introduction The World Medical Association has developed the Declaration of Helsinki as a statement of ethical principles to provide guidance to physicians and other
  • Clinical trials - World Health Organization (WHO)
    The primary Sponsor may or may not be the primary funder The responsible registrant should make every reasonable effort to ensure that a trial is registered once and only once in any one register, and that the trial is registered in the fewest number of registers necessary to meet applicable regulations





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