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Unit-of-Use Pharmaceutical Packaging

Active
Federal

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

General Info

Agency

Department Of Defense → MEDICAL SUPPLY CHAIN FSGBView Agency

NAICS

326199 - All Other Plastics Product ManufacturingView NAICS

Place of Performance

US

Set-Aside

NONE

Documents

(0)

No documents available

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Timeline

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subcontract

Response Deadline

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Organization & Contact Information

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AgencyDepartment Of Defense → MEDICAL SUPPLY CHAIN FSGB
ContactsNo contacts available
OfficeN/A
Organization / Agency
Department Of Defense → MEDICAL SUPPLY CHAIN FSGB
View Agency Profile
Office AddressN/A
ContactsNo contact information available

Full Description

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Supply and assembly of child-proof, non-glass 100cc plastic bottles for pharmaceutical capsule packaging, durable under shipping and handling.

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PHARM MANUF/DISTR DIV - FSAThis contract establishes a nationwide pharmaceutical supply agreement under the Pharmaceutical Prime Vendor (PPV) program, managed by the Defense Logistics Agency Troop Support and the Department of Veterans Affairs, to provide essential medications to the Department of Defense, Veterans Affairs, Bureau of Prisons, and Indian Health Service. The awardee must supply listed pharmaceutical products in accordance with specified quantities estimated in Appendix B, with the contract structured for a one-year base period and four additional option years, totaling a maximum five-year term. Delivery is facilitated through designated PPV contractors, who receive products directly from the awardee and distribute them to government medical facilities; the contractor does not bill the government directly but instead enters into business-to-business agreements with each PPV for payment terms, delivery schedules, and logistics. The contractor is required to have all products registered with RXNorm, First Data Bank, and Medi-Span within five days of award and must comply with strict labeling standards including GS1-128 or HIBCC-compliant barcodes that encode the National Drug Code, lot number, and expiration date, with printing quality meeting ANSI/ISO/IEC Grade C or better. Packaging must feature child-proof closures, meet specific container dimensions, be compatible with automated dispensing systems, and exclude glass bottles. The solicitation is evaluated under a Lowest Price Technically Acceptable (LPTA) methodology, requiring technical acceptability in both compliance with the Statement of Work and demonstrated past performance before price is considered. Offers are deemed technically unacceptable if products lack FDA-approved NDA, ANDA, or BLA status, if manufacturing facilities have unresolved cGMP violations, or if therapeutic equivalence codes are not “A” rated unless all alternatives in the group are “B” rated with submitted bioequivalence data. The contractor must immediately report any FDA warning letters or cGMP inspection failures, and may be restricted from shipping affected products unless granted a 90-day authorization with an approved corrective action plan. Backorders occurring when orders are not fulfilled within 15 days trigger mandatory reporting within four calendar days and may lead to government procurement from alternate vendors, with the contractor liable for any excess costs incurred. The contractor is prohibited from assigning payment rights and cannot initiate claims under the Disputes Clause for disagreements with PPVs. Compliance with the Drug Supply Chain Security Act is mandatory, and adherence to DFARS 252.204-7018 prohibits the use of covered defense telecommunications equipment or services, requiring detailed disclosures of such equipment if applicable. All
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