Attachment No. 10 Section J Protection of Human Subjects Form-0990-0263 2-22.pdf

PDF 88 KB Posted

Attached to
NIMH PSYCHOACTIVE DRUG SCREENING PROGRAM (PDSP)
Solicitation number
NIH-NIMH-75N95023R00003
Issued by

About this file

This document contains a template for certifying compliance with human subjects research requirements on federal contracts and grants. It requests basic proposal information and certification that all human subjects research activities have been reviewed and approved by an Institutional Review Board. Researchers must confirm they have an applicable federalwide Assurance on file with HHS, provide the Assurance identification number and expiration date. If no Assurance is in place, one must be established upon award. Exemptions from IRB review for certain categories of research involving human subjects can also be claimed according to Common Rule criteria. Signatories affirm all future research will undergo continuing IRB review for the duration of each study.

This federal contract opportunity posted by the National Institute of Mental Health seeks proposals to operate the Psychoactive Drug Screening Program, which screens compounds for potential psychoactive effects. The anticipated single award contract will have a one year base period and four one year options, with an anticipated award date of August 6, 2023. Proposals are due under NAICS code 541715 and will be evaluated using FAR Part 15 procedures for negotiated procurements. Interested offerors should review all attachments and contact points of contact with any questions.

View the file

Other files

File Type Posted
Attachment 26 Commitment to Protect Non-Public Information Contractor Agreement.pdf PDF
Attachment No. 25 Public Health Surveillance Exclusion Request.pdf PDF
75N95023R00003 RFP A00002 2.21.23.pdf PDF
Attachment No. 27 Monthly Summary of Sales.pdf PDF
75N95023R00003 A00002 SF30 2.21.23.pdf PDF
Attachment No. 24 PHS Human Subjects And Clinical Trials Info_3_0-V3.0.pdf PDF
Attachment No. 23 Q+A.pdf PDF
75N95023R00003 A00001 SF30..pdf PDF
Attachment No. 2 Proposal Intent Response Sheet.pdf PDF
Attachment No. 18 2015-4281 Wage Determination.pdf PDF
Attachment No. 3 PDSP SOW 05032022.pdf PDF
Attachment No. 17 Offeror Points of Contact.pdf PDF
Attachment No. 13 VPAT2.4RevEU(March2022).pdf PDF
Attachment No. 19 Disclosure of Lobbying 0346 0446.pdf PDF
Attachment No. 14 Subcontracting Plan revised 2017.pdf PDF
Attachment No. 6 CONTRACTOR NON-DISCLOSURE AGREEMENT.pdf PDF
NIH-NIMH-75N95023R00003 RFP.pdf PDF
Attachment No. 20 NIH(RC)1.pdf PDF
Attachment No. 15 Breakdown of Proposed Estimated Cost.xlsx XLSX spreadsheet
Attachment No. 9 Summary of Related Activities.pdf PDF
Attachment No. 11 VAS contracts.pdf PDF
Attachment No. 7 Additional Technical Proposal Instructions.pdf PDF
Attachment No. 16 Financial Questionnaire.pdf PDF
Attachment No. 12 Proposal Summary and Data Record, NIH NIH2043.pdf PDF
Attachment No. 22 Employee Separation Checklist.pdf PDF
Attachment No. 1 Packaging and Delivery of Proposals for Use with the NIH eCPS website.pdf PDF
Attachment No. 8 Tech-Prop-Cost-Summary.pdf PDF
Attachment No. 4 GOVERNMENT FURNISHED PROPERTY.pdf PDF
Attachment No. 21 Suitability Roster.xlsx XLSX spreadsheet
Attachment No. 5 REPRESENTATIONS, CERTIFICATIONS, AND OTHER STATEMENTS OF OFFERORS.pdf PDF
Show all 30

On GovTribe

Work with this file

  • Download the original file
  • Contacts named in this file
  • Similar government files
  • Ask GovTribe AI about this file

Text version

OMB No. 0990-0263 Approved for use through June 30, 2024

Protection of Human Subjects Assurance Identification/IRB Certification/Declaration of Exemption (Common Rule)

Policy: Research activities involving human subjects may not be conducted or supported by the Departments and Agencies adopting the Common Rule unless the activities are exempt from or approved in accordance with the Common Rule. The “pre-2018 Common Rule (or pre-2018 Requirements)” was originally promulgated in 1991 and amended on June 23, 2005 (70 FR 36325). The “2018 Common Rule (or 2018 Requirements)” was originally published on January 19, 2017 (82 FR 7149) and amended on January 22, 2018 (83 FR 2885) and June 19, 2018 (83 FR 28497). The categories of exempt research are provided in Section 101(b) of the pre-2018 Common Rule and Section 104(d) of the 2018 Common Rule.

The pre-2018 Common Rule requires institutions to certify that each application or proposal for research has been reviewed and approved by an Institutional Review Board (IRB) (Section 103(f)). The 2018 Common Rule requires institutions to certify that each proposed research study has been reviewed and approved by an IRB (Section 103(d)). Institutions must have an assurance of compliance that applies to the research to be conducted and should submit certification of IRB review and approval with each application or proposal, or proposed research study, unless otherwise advised by the Department or Agency.

1. Request Type

[ ] ORIGINAL

[ CONTINUATION

[ ] EXEMPTION

2. Type of Mechanism

[ ] GRANT

[ ] CONTRACT

[ ] FELLOWSHIP

[ ] COOPERATIVE

AGREEMENT

[ ] OTHER:

3. Name of Federal Department or Agency and, if known, Application or Proposal Identification No.

4. Title of Application or Activity 5. Name of Principal Investigator, Program Director, Fellow, or Other

6. Assurance Status of this Project (Respond to one of the following)

[ ] This Assurance, on file with the Department of Health and Human Services, covers this activity:

Assurance Identification No. , the expiration date IRB Registration No.

[ ] This Assurance, on file with (agency/dept) , covers this activity.

Assurance No. , the expiration date IRB Registration/Identification No. (if applicable)

[ ] No assurance has been filed for this institution. This institution declares that it will provide an Assurance and Certification of IRB review and approval upon request.

[ ] Exemption Status: Human subjects are involved, but this activity qualifies for exemption under the pre-2018 Common Rule, Section 101(b), paragraph .

[ ] Exemption Status: Human subjects are involved, but this activity qualifies for exemption under the 2018 Common Rule, Section 104(d), paragraph

7. Certification of IRB Review (Respond to one of the following IF you have an Assurance on file)

[ ] This activity has been reviewed and approved by the IRB in accordance with the Common Rule and any other governing regulations.

by:

[ ] Full IRB Review on (date of IRB meeting) or [ ] Expedited Review on (date)

[ ] If less than one year approval, provide expiration date

[ ] This activity contains multiple projects, some of which have not been reviewed. The IRB has granted approval on condition that all projects covered by the Common Rule will be reviewed and approved before they are initiated and that appropriate further certification will be submitted.

8. Comments

9. The official signing below certifies that the information provided above is correct and that, as required, future reviews will be

10. Name and Address of Institution performed until study closure and certification will be provided.

11. Phone No. (with area code)

12. Email:

13. Name of Official

14. Title

15. Signature

16. Date

Authorized for local Reproduction

Sponsored by HHS

According to the Paperwork Reduction Act of 1995, no persons are required to respond to a collection of information unless it displays a valid OMB control number. The valid OMB control number for this information collection is 0990-0263. The time required to complete this information collection is estimated to average 30 minutes per response. If you have comments concerning the accuracy of the time estimate(s) or suggestions for improving this form, please write to: U.S. Department of Health & Human Services, OS/OCIO/PRA, 200 Independence Ave., S.W., Suite 336-E, Washington D.C. 20201, Attention: PRA Reports Clearance Officer.

File details come from the government source that posted it. Updated .