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Central Ethics committee 

  1. ICMR National Ethical Guidelines for Biomedical and health Research involving Human Participants 2017
  2. New Drugs and Clinical Trial Rules 2019
  3. Good Clinal Practice Guidelines for Clinical Trials in Ayurveda, Siddha and Unani Medicine (GCP-ASU)
  4. ICH E6(R3) Guideline for good clinical practice (GCP)
  5. ICH E6(R2) Guideline for good clinical practice (GCP)
  6. ICH E6(R1) Guideline for good clinical practice (GCP)
  7. WHO Handbook for Good clinical Research Practice(GCP) 2000
  8. Surveying and Evaluating Ethical Review Practices WHO 2002
  9. International Ethical Guidelines for Health-related Research Involving Humans(  2016)prepared by  the Council for International Organizations of Medical Sciences (CIOMS) in collaboration with the World Health Organization (WHO)
  10. CCRAS Research Policy
  11. CCRAS General Guidelines for Drug Development of Ayurvedic formulations
  12. CCRAS General Guidelines for safety/toxicity evaluation of Ayurvedic formulations
  13. CCRAS General Guidelines for Clinical Evaluation of Ayurvedic Interventions
  14. CIOMS International Ethical Guidelines for Biomedical Research Involving Human Subjects,2002.
  15. CIOMS Clinical research in resource-limited settings, 2021
  16. WMA Declaration of Taipei on Ethical Considerations regarding Health Databases and Biobanks – WMA – The World Medical Association.

a. List of CEC Members

b. Organogram 

c.  Draft SoP of CEC, CCRAS

d.  Details of Contact person: Dr Renu Singh, Member Secretary, email: dr.renusingh@ccrasnic.in, Mob: 8826570500

e.Research misconduct allegations

f. List Proposals submitted for CEC Approval

g. Department of Health Research (DHR) Registration Certificate of CEC-CCRAS

h. SIDCER FERCAP Survey Visit Certificate of CEC-CCRAS

i. Application/Submission forms for Principal Investigators

j. Proposal Submission Procedure at CEC-CCRAS 

k.   CEC Meeting Schedule

Complaints/Grievance Redressal  Channel

Attachments

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