Quality, compliance, accuracy, reliability and expertise are all critically important in the world of clinical research. With Quorum’s focus on performance – sponsors, CROs and other funding agencies can rely on Quorum Review IRB to safeguard the rights and well-being of research participants while promptly delivering accurate study documents.
Initial SubmissionInformation on how to set up a study with Quorum. |
Study ChangesInformation on which types of changes require submission to Quorum. |
Continuing Review and ClosureInformation regarding continuing review at the protocol level, sponsors continuing review forms and FAQs. |
Safety ReportingInformation about Quorum’s reporting guidelines, forms, and safety reporting FAQs. |
Participant RecruitmentGuidance on creating and submitting recruitment materials. |
Research in CanadaThe North American Board complies with Canadian and U.S. requirements and meets every Wednesday to review U.S. and Canadian studies. |
FAQsCommon questions and information to help avoid obstacles throughout a study. |
Conflict of InterestQuorum’s conflict of interest policy attempts to strike a balance between differing agency standards (e.g., FDA, PHS, Health Canada, etc.), relevant guidance, and accreditation standards related to conflict of interest reporting. |
