English to Russian Medical Medical: Pharmaceuticals

Good Clinical Practice
The investigator will ensure that this study is conducted in accordance with the principles of the “Declaration of Helsinki” International Conference of Harmonisation (ICH) guidelines, and that the basic principles of “Good Clinical Practice,” as outlined in 21 Code of Federal Regulations (CFR) 312, Subpart D, “Responsibilities of Sponsors and Investigators,” 21 CFR, Part 50, and 21 CFR, Part 56, are adhered to.
Investigators and all subinvestigators must provide documentation of their financial interest or arrangements with ХХХХ, or proprietary interests in the drug being studied.
This documentation must be provided before participation of the investigator and any subinvestigator.