Instructions for completing the Clinical Trial Site Information Form

The Clinical Trial Site Information (CTSI) form is required to be submitted by clinical trial sponsors prior to initiating a protocol or implementing subsequent amendment(s) at the clinical trial site for trials that are subject to Division 5 of Part C of the Food and Drug Regulations or the Clinical Trials for Medical Devices and Drugs Relating to COVID-19 Regulations.

Publisher
Health Canada
Resources
2
Catalogue metadata updated
2022-06-07

Data overview

Formats
HTML
File languages
English, French

Official sources and licences

Resources

Related open data