Guidance Document For Clinical Trial Sponsors: Clinical Trial Applications
The Food and Drugs Act and the Food and Drug Regulations govern the sale and importation of drugs for use in human clinical trials in Canada. This document provides guidance on the regulatory obligations pursuant to Part C, Division 5 of the Regulations, Drugs for Clinical Trials Involving Human Subjects.
- Publisher - Current Organization Name: Health Canada
- Licence: Open Government Licence - Canada
Data and Resources
-
Guidance Document For Clinical Trial Sponsors: Clinical Trial ApplicationsHTMLEnglish publication HTML
-
Guidance Document For Clinical Trial Sponsors: Clinical Trial ApplicationsHTMLFrench publication HTML
Similar records