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Connecticut CaRI Database Information

Last Reviewed: Dec. 1, 2023

Connecticut Tumor Registry


Registry jurisdiction Connecticut
Type of review required Local/state IRB review only
IRB of record Connecticut Department of Public Health Human Investigations Committee
How to submit request:
Initial required documentation

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Step-by-Step data request submission process

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Other requirements and helpful information for researchers Patient contact studies may be carried out in collaboration with the Yale Rapid Case Ascertainment Shared Resource (RCA). RCA can also provide assistance with biospecimen research studies and with IRB approval processes. RCA operates on a fee-for-service basis. For further information, go to: https://www.yalecancercenter.org/research/resources/rapid.aspx
Processing timeframe
  • For linkage studies and de-identified data release: 1 - 3 months
  • For patient contact studies: 1 - 3 months
Patient Consent and Contact Procedures
  • Active consent with the physician is required before patient contact. Physician consent is obtained by: Registry
  • Patient consent is obtained by: Researcher
Pediatric research considerations Researchers planning to undertake research involving children should contact the DPH HIC Chair prior to submitting an application. Additional assurances may be required depending on the type of research.
Registry Fees No registry fees
IRB Fees No IRB fees
Collaboration with local researcher required No