Opportunity Information: Apply for DARPA BAA 12 37
Apply for DARPA BAA 12 37
- The DARPA Defense Sciences Office in the science and technology and other research and development sector is offering a public funding opportunity titled "Biologically derived Medicines on Demand (Bio MOD)" and is now available to receive applicants.
- Interested and eligible applicants and submit their applications by referencing the CFDA number(s): 12.910 Research and Technology Development.
- This funding opportunity was created on May 22, 2012 and posted on Mar 21, 2012.
- Applicants must submit their applications by Jun 21, 2012. (Agency may still review applications by suitable applicants for the remaining/unused allocated funding in 2026.)
- Eligible applicants include: Unrestricted (i.e., open to any type of entity above), subject to any clarification in text field entitled Additional Information on Eligibility.
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Opportunity Summary:
The Biologically derived Medicines on Demand (Bio MOD) opportunity is a DARPA Defense Sciences Office research and development effort aimed at shrinking and speeding up the production of protein-based biologic medicines so they can be made when and where they are needed, rather than relying entirely on traditional centralized manufacturing and long supply chains. The core idea is to give military medical teams a way to respond to unpredictable battlefield threats and urgent medical needs by producing different therapeutic proteins on demand, including in far-forward or austere environments where resupply is difficult and time is critical. In practical terms, the program is looking for technologies that can pivot quickly from one biologic to another and deliver usable medicines within short timeframes at or near the point of care.
Bio MOD is built around two main technical thrusts. First, it seeks novel, flexible methods for engineering or modifying biological production systems so they can synthesize multiple protein therapeutics. DARPA explicitly calls out several possible production modalities: engineered microbial strains, engineered eukaryotic strains, and cell-free systems. This indicates an interest in a range of manufacturing approaches, from living cells optimized for rapid expression to cell-free protein synthesis platforms that can avoid some of the logistical burdens of maintaining viable cultures. The emphasis on flexibility and “multiple protein based therapeutics” suggests the government is not looking for a single-purpose factory for one drug, but rather a broadly reconfigurable capability, where the underlying biology and workflow can be adapted to produce different proteins as mission needs change.
Second, the program targets flexible and portable device platforms that can manufacture multiple biologics with high purity, efficacy, and potency at the point of care. That combination of requirements matters because producing a protein is not enough; the output must meet functional quality needs, and the device must be capable of producing therapeutics that perform as intended. The language also highlights speed and portability, implying systems that integrate or simplify steps like expression, processing, and purification in a compact form factor suitable for deployment. Overall, DARPA is aiming at a “fieldable” manufacturing platform that helps medics and operational units generate reliable biologic treatments on site, potentially reducing dependence on cold chains and large inventories while increasing responsiveness to emerging in-theater conditions.
From an administrative standpoint, this is a discretionary federal funding opportunity under DARPA Broad Agency Announcement DARPA BAA 12-37, categorized as Science and Technology and other Research and Development, with CFDA number 12.910 (Research and Technology Development). The program allowed multiple award instruments, including cooperative agreements, grants, other transactions/procurement contracts, reflecting DARPA’s typical flexibility in structuring R&D awards based on the nature of the work and performer. There was no cost sharing or matching requirement listed. Eligibility was described as unrestricted, meaning it was open to any type of entity, subject to any additional constraints in the full announcement. The opportunity was posted March 21, 2012, with an original closing date of June 12, 2012, later extended to June 21, 2012, and it was archived August 21, 2012. For access issues with the announcement, the listed point of contact was COL Geoffrey Ling, BAA Coordinator.
Bio MOD (Biologically derived Medicines on Demand) - FAQ
What is the Bio MOD opportunity?
Bio MOD (Biologically derived Medicines on Demand) is a DARPA Defense Sciences Office research and development effort focused on shrinking and speeding up the production of protein-based biologic medicines so they can be made when and where they are needed, rather than relying entirely on centralized manufacturing and long supply chains.
What problem is DARPA trying to solve with Bio MOD?
The program is aimed at enabling military medical teams to respond to unpredictable battlefield threats and urgent medical needs by producing therapeutic proteins on demand, including in far-forward or austere environments where resupply is difficult and time is critical.
What is the main goal of the program in practical terms?
DARPA is looking for technologies that can pivot quickly from one biologic to another and deliver usable medicines within short timeframes at or near the point of care.
What kinds of medicines are in scope for Bio MOD?
The opportunity focuses on protein-based biologic medicines, described as therapeutic proteins. The emphasis is on being able to produce multiple protein-based therapeutics (not just one product).
Does Bio MOD focus on a single drug or multiple biologics?
Bio MOD emphasizes flexibility and the ability to make multiple protein-based therapeutics. The government is not seeking a single-purpose manufacturing solution for one drug, but a broadly reconfigurable capability that can be adapted as mission needs change.
What are the two main technical thrusts of Bio MOD?
The program is built around two main thrusts: (1) novel, flexible methods for engineering or modifying biological production systems so they can synthesize multiple protein therapeutics, and (2) flexible and portable device platforms that can manufacture multiple biologics with high purity, efficacy, and potency at the point of care.
What production modalities does DARPA explicitly mention?
DARPA explicitly calls out engineered microbial strains, engineered eukaryotic strains, and cell-free systems as possible production modalities.
What does DARPA mean by flexible biological production systems?
Based on the description, flexibility refers to production systems and workflows that can be engineered or modified to switch rapidly between different protein therapeutics, rather than being optimized for only one biologic.
What is a cell-free system in the context of this opportunity?
Within Bio MOD, cell-free systems are described as one of the production modalities of interest and are positioned as platforms that can avoid some logistical burdens associated with maintaining viable cultures, while still enabling protein synthesis.
What does DARPA mean by point-of-care manufacturing?
Point-of-care manufacturing here refers to producing biologic medicines at or near where patients are treated, including potentially in deployed or austere settings, rather than exclusively in centralized facilities.
Why does the opportunity emphasize portability?
Portability is highlighted because the intended operating environments include far-forward or austere locations where resupply is difficult. A portable system supports deployment and use close to the point of care.
What quality attributes does DARPA require from the manufactured biologics?
The device platform thrust explicitly calls for the ability to manufacture multiple biologics with high purity, efficacy, and potency at the point of care.
Is producing a protein alone considered sufficient for Bio MOD?
No. The program description emphasizes that producing a protein is not enough; the output must meet functional quality needs and the therapeutics must perform as intended (including purity, efficacy, and potency).
What does the opportunity suggest about manufacturing steps like purification?
The description implies interest in systems that integrate or simplify steps such as expression, processing, and purification in a compact form factor, consistent with point-of-care use.
What kind of platform is DARPA ultimately aiming for?
DARPA is aiming for a fieldable manufacturing platform that helps medics and operational units generate reliable biologic treatments on site, potentially reducing dependence on cold chains and large inventories while increasing responsiveness to emerging in-theater conditions.
What type of funding opportunity is this administratively?
This is a discretionary federal funding opportunity under a DARPA Broad Agency Announcement (DARPA BAA 12-37), categorized as Science and Technology and other Research and Development.
What CFDA number is associated with this opportunity?
The CFDA number listed is 12.910 (Research and Technology Development).
What award instruments were available under this opportunity?
The opportunity allowed multiple award instruments, including cooperative agreements, grants, and other transactions/procurement contracts, reflecting DARPA's flexibility in structuring R&D awards based on the nature of the work and performer.
Was cost sharing or matching required?
No cost sharing or matching requirement was listed for this opportunity.
Who was eligible to apply?
Eligibility was described as unrestricted, meaning it was open to any type of entity, subject to any additional constraints in the full announcement.
What are the key dates for the opportunity?
The opportunity was posted on March 21, 2012. The original closing date was June 12, 2012, later extended to June 21, 2012. It was archived on August 21, 2012.
What does it mean that the opportunity was archived?
Based on the provided information, archived indicates the opportunity is no longer an active open solicitation and has been closed out in the listings as of August 21, 2012.
Where can applicants find the announcement reference for this opportunity?
The opportunity is tied to DARPA Broad Agency Announcement DARPA BAA 12-37.
Who was the point of contact for access issues with the announcement?
For access issues with the announcement, the listed point of contact was COL Geoffrey Ling, BAA Coordinator.
What is DARPA's organizational component associated with this program?
The Bio MOD effort is identified as a DARPA Defense Sciences Office research and development program.
Does the opportunity indicate a preference for a specific manufacturing approach (microbial, eukaryotic, or cell-free)?
No specific preference is stated in the provided description. DARPA explicitly mentions engineered microbial strains, engineered eukaryotic strains, and cell-free systems, indicating interest in a range of approaches.
Is the program focused on centralized manufacturing or distributed production?
The program is explicitly aimed at enabling on-demand, near-point-of-care production and reducing reliance on traditional centralized manufacturing and long supply chains.
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