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  • IRB Main
    • ICMR Ethical Guidelines
    • New Drugs And Clinical Trial Rule, 2019
    • National Ethical Guidelines for Biomedical Research Involving Children ICMR
    • IRB Calendar
  • Institute Ethics Committee
    • Introduction and term of reference
    • List Of IEC Members
    • Constitution of IEC
    • Standard Operating Procedure
      • Review of study completion reports
      • Site Monitoring
      • Dealing with participants / Patients requests and complaints
      • Vulnerable population
      • Conflict of Interest
      • Management of protocol submission
      • Initial Review of Submitted Protocol
      • Expedited Review of Submitted Protocol
      • Agenda Preparation
      • Review of Amended Protocol / Protocol related documents
      • Continuing review of study Protocols
      • Reporting of Protocol Deviation
      • Review of Serious Adverse Events (SAE) Reports
      • Maintenance of Active Project Files
      • Documentation of the IRB activities
      • Management of premature termination / suspension / discontinuation of the study
      • Social and behavioral studies document and guidelines
  • Conducting research in CIHSR
    • Process for conducting research in CIHSR
    • Responsible Conduct of Research
    • IEC Initial Review Flow Chart
    • Declaration Of Helsinki
  • Forms to Download
  • Study Protocol Format
  • FAQ
  • Contact
logo
Christian Institute of Health Sciences
and Research

Institutional Review Board (IRB)

HOME
  • IRB Main
    • ICMR Ethical Guidelines
    • New Drugs And Clinical Trial Rule, 2019
    • National Ethical Guidelines for Biomedical Research Involving Children ICMR
    • IRB Calendar
  • Institute Ethics Committee
    • Introduction and term of reference
    • List Of IEC Members
    • Constitution of IEC
    • Standard Operating Procedure
      • Review of study completion reports
      • Site Monitoring
      • Dealing with participants / Patients requests and complaints
      • Vulnerable population
      • Conflict of Interest
      • Management of protocol submission
      • Initial Review of Submitted Protocol
      • Expedited Review of Submitted Protocol
      • Agenda Preparation
      • Review of Amended Protocol / Protocol related documents
      • Continuing review of study Protocols
      • Reporting of Protocol Deviation
      • Review of Serious Adverse Events (SAE) Reports
      • Maintenance of Active Project Files
      • Documentation of the IRB activities
      • Management of premature termination / suspension / discontinuation of the study
      • Social and behavioral studies document and guidelines
  • Conducting research in CIHSR
    • Process for conducting research in CIHSR
    • Responsible Conduct of Research
    • IEC Initial Review Flow Chart
    • Declaration Of Helsinki
  • Forms to Download
  • Study Protocol Format
  • FAQ
  • Contact
logo
Christian Institute of Health Sciences
and Research

Institutional Review Board (IRB)

Forms to Download

 ANNEXURE 1
(Cover Letter for Initial Review)
 ANNEXURE 2
(Initial Review Form)
 ANNEXURE 3
(Informed Consent Document)
 ANNEXURE 4
(Curriculum Vitae)
 ANNEXURE 13
(Expedited Review Form)
 ANNEXURE 14
(Exemption from Review)
 ANNEXURE 15
(Continuing Report Form)
 ANNEXURE 16
(Protocol Amendment Form)
 ANNEXURE 17
(Cover Letter for Amendment)
 ANNEXURE 18
(Protocol Violation Form)
ANNEXURE 19
(SAE Form)
 ANNEXURE 20
(Termination Suspension Form)
 ANNEXURE 21
(Social Research Form)
 ANNEXURE 22
(Final Report Form)
 ANNEXURE 23
(Cover Letter for Completed Proposal)
 ANNEXURE 30
(Retrospective Study Form)
 ANNEXURE 31
(Request and issuance of documents)
 ANNEXURE 32
(Confidential agreement of guest)
 ANNEXURE 33
(SOP Amendment Request Form)

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