The Department of Veterans Affairs (VA) is issuing a presolicitation notice for Request for Proposal (RFP) 36E79725R0029 concerning the procurement of Aprepitant Capsules. This unrestricted procurement will cater to various federal entities, including the Department of Defense and the Bureau of Prisons, with the goal of ensuring a continuous supply of the medication. The contract will have a duration of one year plus four optional annual extensions. Offerors must provide a unique National Drug Code (NDC) number and ensure their label is the sole representation on the product.
The solicitation is set to be released around March 25, 2025, with a closing date of April 8, 2025. It emphasizes the necessity for interested parties to stay updated via the SAM.gov website, as no paper copies will be provided. The estimated annual requirements indicate substantial quantities of Aprepitant in various dosages, highlighting the importance of this procurement in serving veterans and other federal health care facilities. Matthew Poulin serves as the point of contact for inquiries regarding this solicitation, reinforcing communication between the VA and potential offerors for clarification and submission processes.
The document is a Request for Proposal (RFP) from the Department of Veterans Affairs for supplying various pharmaceutical products, specifically Aprepitant capsules, under a contract aimed at ensuring availability and committed-use pricing for government participants, including Veterans Affairs, Department of Defense, and Indian Health Service facilities. Offerors must provide prices for multiple line items covering the base year and four option years, with conditions set for pricing, including a 0.5% Cost Recovery Fee. To be eligible, contractors must submit necessary documentation including National Drug Codes (NDCs) and letters of commitment from manufacturers if they are not the manufacturers themselves. The contract's focus includes compliance with pharmaceutical standards and regulations, including adherence to Drug Supply Chain Security Act (DSCSA) requirements. Contractors are required to maintain cGMP (current Good Manufacturing Practices), and products must have appropriate labeling and packaging. The document outlines the evaluation, agreement terms, pricing mechanisms, and compliance assessments necessary for successful proposals, emphasizing the necessity of timely and accurate submissions and the importance of operational agreements with Prime Vendors for distribution.