Clinical Trial Site Information Form - Canada (English / French)

The Clinical Trial Site Information Form - Canada (English/French) is used to collect information about the sites where clinical trials will take place in Canada. It helps ensure that the trials are conducted in accordance with applicable regulations and guidelines.

The clinical trial site information form in Canada is typically filed by the site principal investigator or the institution's research team.

FAQ

Q: What is the Clinical Trial Site Information Form?
A: The Clinical Trial Site Information Form is a document used to collect information about the site where a clinical trial is conducted.

Q: What is the purpose of the form?
A: The form is used to gather important details about the site, such as its location, facilities, and staff qualifications.

Q: Who should fill out the form?
A: The form is typically completed by the site's principal investigator or designated representative.

Q: Is the form available in multiple languages?
A: Yes, the form is available in both English and French to accommodate users in Canada.