OUR ADVANTAGE

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
 

 

LATEST NEWS
  • 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
CLINICAL INVESTIGATOR REGISTRY FORM
 
INVESTIGATOR PERSONAL INFORMATION
Name*
Date of Birth*
Current Empolyment Status
Full Address of *
Hospital / Institute / Clinic
City*
  Pin*
Country
  Phone*
Fax
  Mobile*
Email*
  Website
INVESTIGATOR EDUCATION
Medical Qualification*
Medical Registration No*
School / Institution
Degree   Year Graduated
Post Graduation
Degree   Year Graduated
THERAPEUTIC AREA / AREAS
Additional Training
Degree   Year Completed
Comments
INVESTIGATOR HOSPITAL AFFILIATIONS
Primary Hospital*
Address*
Contact Name
Phone
    Fax
Mobile
  Email
Affiliation Name
Comments
Any other Hospital
CLINICAL RESEARCH EXPERIENCE
Are you interested in conducting Clinical Trials* Yes No
Have you conducted Clinical Trials?* Yes (If Yes, specify details below) No
Details of Clinical Trials conducted (Phase, Duration, Therapeutic area etc)
GCP Trained* Yes No
Association with any Ethics Committee?* Yes No
Approximate No. of patient pool in
respective theraupetic area
Any other details if any
 
 
 
 
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