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World Health Organization regulatory activities

United States, Australia, Canada, the Nordic countries, and the World Health Organization (WHO). The ICH guidance defines QA as All those planned and systematic actions that are established to ensure that the trial is performed and the data are generated, documented (recorded), and reported in compliance with GCP and the applicable regulatory require-ment(s). Quality control, on the other hand, is defined as The operational techniques and activities undertaken with the QA system to verify that the requirements for quality of the trial-related activities have been fulfilled. [Pg.3071]

See other pages where World Health Organization regulatory activities is mentioned: [Pg.341]    [Pg.442]    [Pg.544]    [Pg.2]    [Pg.129]    [Pg.569]    [Pg.1788]    [Pg.136]    [Pg.936]    [Pg.617]    [Pg.828]    [Pg.113]    [Pg.347]    [Pg.383]    [Pg.18]    [Pg.391]    [Pg.460]    [Pg.326]    [Pg.279]    [Pg.35]    [Pg.97]    [Pg.227]   
See also in sourсe #XX -- [ Pg.222 , Pg.227 ]



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