6509--Solifenacin Tabletes (VA-25-00037090)
ID: 36E79725R0020Type: Presolicitation
Overview

Buyer

VETERANS AFFAIRS, DEPARTMENT OFVETERANS AFFAIRS, DEPARTMENT OFNAC PHARMACEUTICALS (36E797)HINES, IL, 60141, USA

NAICS

Pharmaceutical Preparation Manufacturing (325412)

PSC

DRUGS AND BIOLOGICALS, VETERINARY USE (6509)
Timeline
    Description

    The Department of Veterans Affairs (VA) is preparing to issue a Request for Proposal (RFP) for the procurement of Solifenacin Tablets, aimed at ensuring a reliable supply for the VA, Department of Defense (DoD), and other federal health agencies. This unrestricted procurement will award one contract with a term of one year plus four optional renewal periods, requiring offerors to provide specific labeling, packaging details, and compliance with the Drug Supply Chain Security Act. The estimated annual requirements include various packaging sizes and quantities of Solifenacin, reflecting the VA's commitment to maintaining a consistent supply of essential medications for veterans and associated healthcare providers. Interested vendors should monitor SAM.gov for the solicitation release on or around March 14, 2025, with a response deadline of March 28, 2025; inquiries can be directed to Kenneth Lay at Kenneth.Lay@va.gov or by phone at 708-786-4879.

    Point(s) of Contact
    Kenneth LayContract Specialist
    (708) 786-4879
    Kenneth.Lay@va.gov
    Files
    Title
    Posted
    The document outlines a solicitation for pharmaceutical products to be supplied to the Department of Veterans Affairs and other authorized entities such as the Department of Defense and Indian Health Service. The primary purpose is to establish a contractual agreement that ensures the availability and pricing of specific drugs, including Tadalafil tablets in various dosages. Offerors are required to submit competitive pricing for the base year and four option years, including a 0.5% Cost Recovery Fee embedded in all prices. The contract mandates compliance with the Drug Supply Chain Security Act and includes stipulations regarding product registration, packaging, and reporting requirements. Additionally, there is a focus on manufacturers maintaining Good Manufacturing Practices (GMP) to ensure quality and safety. The contract will be administered through Prime Vendor Programs, which facilitate pharmaceutical distribution to several government participants. The document emphasizes objectives such as ensuring consistent product availability, compliance with regulations, and establishing business relationships between contractors and prison facilities. It serves as a comprehensive framework for vendors to understand submission expectations, product specifications, and compliance requirements for effective contract execution.
    The Department of Veterans Affairs (VA) is planning to issue Request for Proposal (RFP) 36E79725R0020 for the procurement of Solifenacin Tablets, aiming to secure a reliable supply for the VA, Department of Defense (DoD), and other federal health agencies. This unrestricted procurement will award one contract, with a term of one year plus four optional renewal periods. Offerors must provide specific labeling and packaging details, including unique NDC numbers and safety-cap requirements for the bottles. The RFP will be made available electronically on or around March 14, 2025, with a response deadline of March 28, 2025. Each interested vendor is encouraged to monitor SAM.gov for updates and potential amendments. Estimated annual requirements include various packaging sizes and quantities of Solifenacin, demonstrating the VA's commitment to streamlined procurement of essential medications for veterans and associated healthcare providers.
    The document outlines a solicitation for the Department of Veterans Affairs (VA) to procure certain pharmaceutical products through its VA Pharmaceutical Prime Vendor (PPV) Program. The main objective is to establish competitive national contract prices for specified drugs, including Solifenacin Succinate tablets, ensuring consistent availability across various VA and Department of Defense healthcare facilities. The solicitation requires bidders to submit prices for both the base year and four option years, adhering to stringent requirements regarding drug sourcing, packaging, and compliance with the Drug Supply Chain Security Act (DSCSA). Participants must provide unique National Drug Code (NDC) numbers for each product, maintain Good Manufacturing Practices (cGMP) as certified by the FDA, and report sales quarterly, including a Cost Recovery Fee of 0.5%. Amendments are included to correct the solicitation, but the offer due date remains the same. The winning contractor will receive orders through the PPV, emphasizing the importance of robust vendor agreements and inventory management. This initiative reflects the government's commitment to ensuring effective procurement processes and healthcare delivery while adhering to federal regulations.
    Lifecycle
    Title
    Type
    Presolicitation
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