… SOP 701.004 SOP 701.004 – Informed Consent Form Requirements and Documentation Page 1 of 13 Title … REB Chair or designee is responsible for reviewing consent forms or changes to consent forms if the changes meet the … that it contains adequate information to safeguard the privacy and confidentiality of research participants; 5.1.3 …
… human participant research in compliance with applicable regulations and guidelines. 3.0 RESPONSIBILITIES All … must make available to the REB their current CV and medical license number (if applicable) and their relevant … to conduct this research, • The Researcher has sufficient space and resources to conduct this research; 5.1.6 Any …
… of all regulatory binders including the REB approval documentation, REB approved consent documents, signed consent documents, correspondence between …
… met. 4.0 DEFINITIONS See Glossary of Terms. 5.0 PROCEDURE Health Canada has the authority to inspect Researcher sites … will confirm with the Sponsor and/or the Researcher (or inspector/auditor, as applicable) regarding the agreed dates …
