Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Good clinical practice obligations

Review of good clinical practices and investigator and staff obligations... [Pg.454]

Good Clinical Practice (GCP) regulations in the United States and the ICH guidelines, which meet safety, ethical and efficacy requirements, are comprehensively covered in the clinical research development chapters. Investigator, sponsor, and monitor obligations are detailed and applied practically. Institutional Review Boards (IRBs), Independent Ethics Committees (IECs), and Informed Consent (IC) will be discussed fully along with the... [Pg.574]


See other pages where Good clinical practice obligations is mentioned: [Pg.502]    [Pg.325]    [Pg.1925]    [Pg.27]    [Pg.638]    [Pg.413]    [Pg.434]    [Pg.2875]    [Pg.140]   
See also in sourсe #XX -- [ Pg.1925 ]




SEARCH



Clinical practice

Good practices

Obligate

Obligations

© 2024 chempedia.info