Integrated Resource Inc (IRI) is a nimble and efficient Clinical Research Organization (CRO) committed to provide comprehensive clinical research solutions to Pharmaceutical, Biotechnology and Medical device companies. IRI specializes in clinical data management (CDM) solutions for clinical trials in early phase (Phase I & II) or late phase (Phase III & IV) of drug development i.e. Interventional & Observational trials.
Integrated Resources is committed to effectively reduce the time and cost it takes to go from the protocol design phase to initial data analysis, while delivering consistent quality on-time and on-budget. Its operational standards are set-up with objective to closely follow and implement industry guidelines (& regulations) such as FDA’s 21 CFR part 11, ICH GCP, SCDM’s GCDMP & CDISC standards.