The CRID identifier was conceived and developed by Gerry Nesbitt [bio↗] in 2019. He saw the need for a single patient identifier that could link disparate datasets in rare disease clinical research. Prior to CRID, the alternative was to link datasets using patients' personally identifiable information (PII), which wasn't always possible due to stringent privacy regulations. National identifiers (e.g. social security number) and patients' hospital identifiers were not feasible as these too were sensitive pieces of PII that would have security and privacy concerns like healthcare fraud, reduced privacy, coercive surveillance, and many more. There is also a concern that not all of a patient's medical data should be connected to a single identifier. For Nesbitt, the obvious solution was to empower the patient (or parent of a child) to create their own identifier that could be used specifically for clinical research. The CRID (clinical research ID) was born.
Gerry Nesbitt MBA Dip.CorpFin PMP, CEO, CLIRINX Ltd. & CRID™
A patient-generated unique identifier to breakdown data-silos and promote data sharing.
CRID is 100% owned and managed by CLIRINX Ltd, a clinical research IT company based in Ireland. We would welcome a proposal from an appropriate organization(s) interested in acquiring and overseeing the CRID system.
Mar 7th, 2024
NR2F1 Foundation | Webinar | CRID with Gerry Nesbitt
Mar 1st, 2024
Creating a New Account is now a 2-step process to help ensure all email addresses are genuine.
Jan 16th, 2024
Cure GABA-A | Launch and Learn | CRID with Gerry Nesbitt
Sept 21st, 2022
CRID RESTful API Launched
Aug 23rd, 2022
CRID Training Video
Dec 2nd-6th, 2022
American Epilepsy Society Meeting (Nashville, TN)