serving the needs of study sponsors
Home › Sponsors/CROs
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 Submission
Information on how to set up a study with Quorum.
Study Changes
Information on which types of changes require submission to Quorum.
Continuing Review and Closure
Information regarding continuing review at the protocol level, sponsors continuing review forms and FAQs.
Safety Reporting
Information about Quorum's reporting guidelines, forms, and safety reporting FAQs.
Participant Recruitment
Guidance on creating and submitting recruitment materials.
Research in Canada
The North American Board complies with Canadian and U.S. requirements and meets every Wednesday to review U.S. and Canadian studies.
FAQs
Common questions and information to help avoid obstacles throughout a study.