| PRESOLICITATION NOTICE Development of Radiation/Nuclear Medical Countermeasures (MCMs) or Biodosimetry Devices BAA-75N93022R00021 Presolicitation Notice Information
Introduction
The National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of
Health (NIH), Department of Health and Human Services (HHS) has been charged by the
HHS with developing products for the assessment, diagnosis, mitigation and/or treatment of
radiation injuries resulting from a radiological or nuclear incident, to advance these
approaches to the stage where they are competitive for advanced product development by
the Biomedical Advanced Research and Development Authority (BARDA) or acquisition
under the Project BioShield Act of 2004.
Description
NIAID intends to solicit proposals for contracts entitled "Development of Radiation/Nuclear
Biodosimetry Devices and Medical Countermeasures (MCMs)" to advance the development
of candidate biodosimetry signatures/devices or MCMs to assess injuries and/or reduce
mortality and/or major morbidities associated with exposure to radiation during a radiation
public health emergency. NIAID anticipates that research and development studies
supported by this Broad Agency Announcement (BAA) will advance lead biodosimetry
signatures and devices or candidate MCMs toward eventual FDA clearance, approval, or
licensure. For this BAA, it is anticipated that candidate biodosimetry signature or lead MCMs
will enter the evaluation and development pathway at various stages, from mid-stage
research to post-marketing (for assays/tests or drugs/biologics that are already licensed or
approved for other indications), so the offeror is expected to provide a Statement of Work
(SOW) based on the stage of the candidate and the work that needs to be performed to
advance the biodosimetry signature/device or lead MCM.
Proposals will be evaluated on the availability of data supporting detection of exposure or
prediction of radiation injuries or the amelioration by a candidate MCM of radiation-induced
tissue damage and reduction of mortality and/or major morbidities. Also considered will be
the adequacy of the proposed scientific approach and methodology used to support the
advancement of the candidate biodosimetry signature/device or MCM for the diagnosis,
mitigation or treatment of the acute radiation syndrome (ARS) or delayed effects of acute
radiation exposure (DEARE) toward U.S. FDA approval, licensure, or clearance (under the
FDA Biodosimetry Guidance or the FDA Animal Rule for MCMs). The evaluation will also be
based on the adequacy of the scientific and technical personnel, facilities, equipment, GLP,
cGMP compliance (if applicable) and project management.
It is anticipated that 1-2 cost reimbursement, completion type contracts will be awarded for
a 3-year period of performance beginning on or about March/April 2024.
NIAID estimates that the average annual total cost (direct and indirect costs combined) for
a non-severable base period and each subsequent, non-severable, completion option period
will average $2 million, for a total award of up to $6 million over three years. However, it is
anticipated that the total cost for the award(s) may vary depending upon the scope of the
project and the technical objectives of the award(s). The length of time for which funding is
requested should be consistent with the nature and complexity of the proposed research.
In no event shall the period of performance proposed by an offeror exceed 3 years.
Any responsible offeror may submit a proposal which shall be considered by the Agency.
This BAA will be available electronically on/about November 28, 2022 and may be accessed
through Sam.gov. This notice does not commit the Government to award a contract. No
collect calls will be accepted. No facsimile transmissions will be accepted.
For this solicitation, the NIAID requires proposals to be submitted via the NIAID electronic
Contract Proposal Submission (eCPS) website. Submission of proposals by facsimile or email is not acceptable.
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