Site Identification, Feasibility, Selection & Site Management

IRL Research has developed robust Site Management capabilities over the last 5 years. We understand the importance of Investigator and Site Selection for any given clinical trial. we have developed a database of over 500 potential Investigators in India. A customized feasibility assessment sheet is prepared for each trial and sent to potential investigators. The Site selection process takes into account investigator interest, investigator experience in clinical trials, number of subjects that can be recruited, availability of trained site personnel, facilities, infrastructure and other specific needs related to a particular trial. Pre-qualifying site visits are undertaken at the behest of the sponsor.

IRL Research specializes in:

  • Feasibilities and site identification
  • Site qualification visits
  • PI budgets and contracts
  • Collection of site documents
  • Preparation of EC dossier
  • EC submissions and approvals
  • Coordination of investigator meeting
  • Creation of source document template
  • Recruitment planning
  • Site start up
  • Study conduct at exclusive sites
  • Qc at site
  • Coordinate archiving