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Chemistry, Manufacturing and Controls and Related Services for Development of Drug Products   8

ID: 75N95023R00037 • Type: Solicitation • Match:  100%
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Description

The Therapeutic Development Branch (TDB) within the Division of Preclinical Innovation (DPI) at the National Center for Advancing Translational Sciences (NCATS) conducts translational research in the area of human therapeutics development.

The scope of this contract is for Chemistry, Manufacturing, and Control (CMC) services for Drug Products. The objective of these support services is to ensure receipt of formulated Drug Product (DP) of sufficient quality and quantity to support preclinical, IND-enabling and clinical studies.

The Contractor shall provide support for a broad range of preclinical services required for the design, development, manufacture, and release of DP, and release of DP as Clinical Trial Material (CTM), including precursors, preliminary states, Reference Standards (RS) and all required testing. Ancillary products (e.g., placebos, diluents, adjuvants, master cell banks, testing standards, reference materials) and other materials manufactured or purchased to support clinical trials or CMC activities may also be required. All activities preliminary to manufacturing in accordance with current Good Manufacturing Practice (cGMP) may be required (e.g., development or engineering lots, formulation studies), even without an associated cGMP manufacturing task. All activities required to maintain material in a usable state, including storage, shipping, testing (in process, release, stability, and quality actions), and preparation of documents to support regulatory submissions may also be required.

Product formats may include small molecules, short oligomeric compounds, biological (large) molecules, quaternary molecular assemblies (homogenous or heterogenous), vectors for gene therapy, nanoparticles, and any of the above modified genetically, biologically, or chemically. Novel formats identified after this draft might also be needed. Formats could also include Devices or Combination Products.

The breadth of this Statement of Work (SOW) includes capabilities to support a range of activities differing in size, complexity, and duration.

All applicable attachments in connection with this solicitation are available for download.

Overview

Response Deadline
Aug. 18, 2023, 3:00 p.m. EDT (original: Aug. 4, 2023, 3:00 p.m. EDT) Past Due
Posted
June 20, 2023, 10:01 p.m. EDT (updated: July 17, 2023, 5:50 p.m. EDT)
Set Aside
None
Place of Performance
United States
Source

Current SBA Size Standard
1300 Employees
Pricing
Multiple Types Common
Est. Level of Competition
Average
On 6/20/23 National Institute on Drug Abuse issued Solicitation 75N95023R00037 for Chemistry, Manufacturing and Controls and Related Services for Development of Drug Products due 8/18/23. The opportunity was issued full & open with NAICS 325412 and PSC AN12.
Primary Contact
Name
Michelle Cecilia   Profile
Phone
(301) 827-7199

Secondary Contact

Name
Valerie Whipple   Profile
Phone
(301) 827-5218

Documents

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Additional Details

Source Agency Hierarchy
HEALTH AND HUMAN SERVICES, DEPARTMENT OF > NATIONAL INSTITUTES OF HEALTH > NATIONAL INSTITUTES OF HEALTH NIDA
FPDS Organization Code
7529-75N950
Source Organization Code
100189048
Last Updated
Sept. 2, 2023
Last Updated By
michellececilia.cecilia@nih.gov
Archive Date
Sept. 2, 2023