0% found this document useful (0 votes)
17 views

3.adhoc Codal Documents

Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
0% found this document useful (0 votes)
17 views

3.adhoc Codal Documents

Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PDF, TXT or read online on Scribd
You are on page 1/ 2

S. No.

Name of the Document

1 *
Declaration & Attestation Form (duly signed by Head of Department/ Director)

2 *
Non submission to other agency

3 *
Undertaking of Proposal limits

4 *
Research Experience of PI during last 10 years

5 *†
Certificate of previous ICMR Project

6 *†
Non-availability of Equipment Form (applicable when you are asking equipment grant)

7 *†
NGO Registration Certificate on DARPAN Portal (Applicable only for NGO)

#
8 Justification of Staff, Equipment, Contingency and Travel Allowance

#
9 Scientific and Industrial Research Organisation (SIRO) OR Department of Scientific and
Industrial Research (DSIR) Certificate (if any government organization is exempted for
DSIR/SIRO certificate then exemption certificate duly signed by the Head of the Institute to
be provided )

#
10 Case Record proforma, study instruments, questionnaires, scales, etc

#
11 Mandate Form (duly signed by account officer)

#
12 Undertaking from Institute

#
13 Financial Conflict of Interest by the Investigators

#
14 A certificate to the effect that no utilization certificate/final report is pending for earlier
projects under the PI
#
15 Institutional Ethics Committee) (Human) (undertaking for non requirement of ethics
approval whichever appropriate


16 Review Committee on Genetic Manipulation (RDNAT)- Recombinant DNA technology


17 Clearance from Nuclear Medicine Committee, BARC (If using radio tagged material)


18 Institutional Committee for Stem Cell Research


19 Institutional Bio-safety Committee – Radio Isotopes (RI)


20 Institutional Animal Ethics Committee


21 Drugs Controller General of India (DCGI) Approval - Drug Discovery, Clinical Trial etc.
where DCGI approval is needed


22 Informed Consent Form

Note:
* Mandatory Document at the Proposal submission of the Adhoc project.
#
Mandatory Document when Adhoc proposal is technically approved

Mandatory Document if the Adhoc proposal pertains to the Name of the document

You might also like