Model Acts Program
Program Funding
Annual program obligations reported to SAM.gov.
Program Objective
The purpose of the Model Acts Program includes: A) advising states on establishing laws and policies
to address illicit drug use issues and (B) revising such model state drug laws and draft supplementary model state laws to take into consideration changes in illicit drug use issues in the state involved.
Eligibility
Eligible Applicants
- Nonprofit Organization
Applicants must have expert knowledge and extensive experience in conducting research and analysis, providing technical assistance, and drafting model state drug laws, policies and programs. Applicants must also ensure compliance with all federal laws, regulations, Executive Orders, and public policies governing financial assistance awards.
How to Apply
Award Procedure
Upon approval by ONDCP, a grant letter and conditions are sent to the grantee electronically.
Decision Timeline
- Approval: From 30 to 60 days
Program details & compliance
Description
The Model Acts Program serves to advise States on establishing and updating laws and policies tailored to illicit drug use issues within their States.
Mission Categories
Primary: Legal Services - Other
Use of Funds
Allowed Uses
ONDCP is seeking a provider to:
conduct research and analysis on state and local drug laws, policies and programs;
draft comprehensive model state drug legislation, revise current model laws and draft supplementary model state laws; and
provide technical assistance and maintain a repository and web-based resource center on model state drug laws, policies and programs.
Required Documentation
Applicants must have expert knowledge and extensive experience in conducting research and analysis, providing technical assistance, and drafting model state drug laws, policies and programs.
Reporting & Compliance
Applicable 2 CFR 200 Subparts
- Subpart B — General Provisions
- Subpart C — Pre-Federal Award Requirements
- Subpart D — Post-Federal Award Requirements
- Subpart E — Cost Principles
- Subpart F — Audit Requirements
Formula
Authority: 21 U.S.C. 1706; 21 U.S.C. 1703(d), 1703(f), 21 U.S.C. 1701, 21 U.S.C. 1521-1548, 21 U.S.C. 2001-2003, Office of National Drug Control Policy Reauthorization Act of 2006, P.L 109-469 (2006), 2 CFR part 200.
Source: 79 FR 76105, Dec. 19, 2014, unless otherwise noted.
§ 3603.1 Adoption of 2 CFR Part 200.
Under the authority listed above, the Executive Office of the President, Office of National Drug Control Policy (ONDCP) adopts the Office of Management and Budget (OMB) Guidance in 2 CFR part 200. Thus, this part gives regulatory effect to the OMB guidance and supplements the guidance as needed for ONDCP.