This is a pre-solicitation notice for an unrestricted procurement of Denosumab injection for the Department of Veterans Affairs (VA) and other federal agencies. The VA intends to issue a Request for Proposal (RFP) with an estimated issue date of April 17, 2026, and a tentative closing date of May 5, 2026. The contract will be for one year with four one-year option periods. Offerors must provide an uninterrupted source of supply and state the exact name on the label with a unique NDC number. The NAICS code is **** documents will be available electronically on SAM. gov. The point of contact is Ray Roldan, with questions to be emailed to ***@***. *. * of covered drugs must have established Federal Ceiling Prices (FCPs) and be on file with the VA National Acquisition Center. Proposed biosimilar products must meet FDA criteria and be listed in the FDA purple book. If an offeror markets both vial and syringe presentations for the same product strength, both must be included in the proposal at the same price.
The bid notice does not specify a delivery deadline for the products.
The bid notice does not specify payment terms.
The bid notice does not specify warranty information.
The bid notice states that the VA will award one contract to the responsible offeror who will be able to provide an uninterrupted source of supply for the contracted items.
The bid notice states that offers of covered drugs including biologics that fall within 21 CFR **** will only be considered for award if the offeror has an executed MA and PPA which includes the offered NDC's on file with the VA National Acquisition Center, FSS in accordance with 38 **** H 2. Furthermore, in order to be considered for award under this solicitation, all proposed covered drug product's must be present on the offeror's FSS contract or interim agreement with an established permanent FCP associated with the offeror's FSS contract or interim agreement by this solicitation's due date and time for receipt of offers. Offers failing to meet these criteria will be rejected and receive no further consideration. Proposed biosimilar products must be biological products licensed by the FDA under 42 U. S. C. 262 and must meet all biosimilar criteria described in 42 U. S. C. 262.
The bid notice does not specify penalties.
The bid notice does not mention a site visit.
The bid notice does not mention sample submission.
The bid notice does not specify a challenge deadline.
The bid notice does not provide an estimated total value for the procurement.