Clinical trials require strict adherence to protocol, extensive documentation, complete accuracy, compliance to ICH-GCP and other regulatory norms, an ethically sound patient recruitment strategy, and efficient site management.


QUICK LINKS          
CRP Course I5 Site List
Scheldule Y CDSCO Website
GCP E6 Guideline FDA Guidance


  • CDSCO issues diretion to Zonal Offices for conduction inspection of clinical trial site
  • Clinical trial industry is no killing machine: G.N. Singh - Livemint
  • Draft Guideline of FDA on Electronic Source Capturing
  • ICH makes progress on ongoing reforms and adopts Guidelines for safety reporting. Press Release - ICH Steering Committee, San Diego, California, USA, November 2012
  • DCGI initiates surprise inspection drive on CROs across India
  • Recent draft guidelines release by DCGI for public review and opinion
  • I5 Clinical Research launches FREE GCP Accreditation Test (GAT) for Clinical Research Professionals
  • I5 Clinical Research launches Clinical Research Professional (CRP) Course
  • INC Research to acquire Kendle International
  • Nautic purchase of Omnicare Clinical Research part of recent acquisition trend of mid-sized CROs

I5 has Capabilities to cover almost all indication strating from Oncology to Allergic Diseases.

If you are looking for a specialist not listed here, please contact us to discuss your specific needs. Our vast network and relationships throughout the India will allow us to identify and present qualified specialists that may not be listed.


  Cardiovascular Diseases   Obstetrics & Gynecology
  Dentistry   Opthalmology
  Dermatology   Orthopedics
  Endocrinology   Oncology
  Gstroenterology   Otolaryngology
  General Surgery   Pediatrics
  Hematology   Psychiatry
  Internal Medicine   PulmonaryDisease
  Nephrology   Rheumatology
  Neurology   Urology
  Neurological Surgery  

For confidential purpose name and contact numbers of our investigators are not disclosed. Please contact us for any details regarding our specialist.





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