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IPSEN BIOPHARMACEUTICALS, INC.,

Subsidiary ofIPSENUEI: YJTQU9382HU5

IPSEN BIOPHARMACEUTICALS, INC., is a federal contractor, registered under UEI YJTQU9382HU5. It has been awarded $64,034 across 16 federal contracts. Primary work spans Pharmaceutical Preparation Manufacturing. Top awarding agencies include Department Of Veterans Affairs.

Contact Information

Registration and classification details

Registration

UEI Code

YJTQU9382HU5

Federal Contracting Overview

Award totals, agency breakdown, NAICS distribution, and geographic footprint.

AI Capability Profile

Ipsen Biopharmaceuticals Inc. specializes in the manufacturing of pharmaceutical preparations, with a focus on delivering specialized drug products and hematological therapeutics to federal healthcare systems. Their technical expertise lies in GMP-compliant production processes, drug formulation, an...

Ipsen Biopharmaceuticals Inc. specializes in the manufacturing of pharmaceutical preparations, with a focus on delivering specialized drug products and hematological therapeutics to federal healthcare systems. Their technical expertise lies in GMP-compliant production processes, drug formulation, and the supply chain management of complex biopharmaceuticals, including those used in oncology and rare disease treatment. The company demonstrates deep competency in meeting stringent regulatory standards for sterile and non-sterile drug manufacturing, ensuring consistent quality and traceability across batch production. Their ability to support long-term government supply agreements suggests strong operational scalability and adherence to FDA and VA-specific pharmaceutical compliance frameworks. The contractor maintains a consistent relationship with the Department of Veterans Affairs, providing critical pharmaceuticals under both blanket purchase agreements and Federal Supply Schedule contracts. Their work supports VA’s mission to deliver reliable, uninterrupted access to specialty medications for veteran populations, particularly in areas such as hematology and chronic disease management. This recurring engagement reflects a trusted partnership built on regulatory reliability, consistent product availability, and alignment with VA’s formulary and distribution protocols. Ipsen operates primarily within NAICS 325412, which encompasses the manufacturing of finished pharmaceutical products from active pharmaceutical ingredients. Their market positioning centers on niche therapeutic areas requiring precise formulation and controlled distribution, positioning them as a qualified supplier for federal agencies managing complex drug regimens. They are not a broad-spectrum distributor but a specialized manufacturer focused on high-integrity, clinically essential medications. As a 2L entity headquartered in Cambridge, Massachusetts, Ipsen Biopharmaceuticals Inc. is structured as a mid-sized manufacturer with a focused government market presence. The company holds no formal government certifications but maintains operational compliance through rigorous internal quality systems aligned with federal pharmaceutical standards. Their geographic proximity to major biopharma hubs enhances their ability to collaborate with federal research and procurement networks.

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Award Analytics & Distribution

Awards by Agency
Department Of Veterans Affairs$64.0K100%
Awards by NAICS
325412 - Pharmaceutical Preparation Manufacturing$64.0K100%
Awards by Agency Over Time
Awards by Place of Performance

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NAICS: 811210
New
Federal
OMNICELL MAINTENANCE AND SUPPORT-INTENT TO SOLE SOURCE
Solicitation # 36C24627Q0032
The Department of Veterans Affairs, Network Contracting Office 6, intends to award a one-year, firm-fixed-price contract to Omnicell INC for the FY27 Annual Service Agreement. This requirement, identified by solicitation number 36C24627Q0032 and NAICS code 811210, is estimated to be valued at 163,518.00 dollars. The contract covers the maintenance and support of existing Omnicell equipment located at the Hampton VA Medical Center in Virginia and its associated area clinics. The scope of work includes scheduled and emergency maintenance, preventative maintenance, on-site repair support, software upgrades, and the replacement of hardware components such as batteries, filters, and bulbs, as well as monthly reporting and auditing. The award is being pursued as a sole source procurement under FAR 8.405.6 and FAR 13.106-1(b) because Omnicell INC is the original equipment manufacturer and the sole authorized provider capable of maintaining the equipment and preserving existing warranties. To ensure quality and security, all maintenance must be performed by OEM-trained technicians with the necessary credentials to access proprietary software and manuals. While this is a notice of intent and not a request for competitive quotations, interested parties were invited to identify their capabilities by September 16, 2026. The primary point of contact for this action is Contracting Specialist Kenneca Crump.
Department Of Veterans Affairs

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NAICS: 325412
New
Federal
SNS Pharmaceutical Logistic Replenishment Requirement
Solicitation # 75A50326R00007
The Department of Health and Human Services, through the Administration for Strategic Preparedness and Response, is soliciting proposals under solicitation 75A50326R00007 for the replenishment of expired or expiring pharmaceuticals for the Strategic National Stockpile. This is a full and open competition resulting in a twelve-month Firm Fixed Price contract. The scope includes the procurement of various FDA-approved pharmaceuticals, such as Dopamine Hydrochloride, Norepinephrine, and Morphine Sulfate, with the government reserving the right to increase awarded quantities by up to 20 percent. Deliveries are FOB Destination and may be required at up to nine locations across the contiguous United States and Hawaii. Award decisions will be based on a best-value tradeoff, prioritizing technical capability and past performance significantly over price. Technical evaluation focuses on product compliance, regulatory requirements, and the ability to meet delivery schedules. Strict quality standards are mandated, including adherence to current Good Manufacturing Practice regulations, specific temperature controls between 20C and 25C during storage and transit, and a requirement that products retain at least 90 percent of their FDA-approved shelf life upon receipt. Proposals must be submitted in two volumes by September 18, 2026, including a technical volume, a pricing volume, and a proposal submission worksheet. Large businesses are additionally required to submit subcontracting plans via the SBCX system.
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