Indian Army Department Of Military Affairs Cell Culture Rabies Vaccine, Insulin Syringe & ECG Paper Tender 2025
Indian Army
DEHRADUN, UTTARAKHAND
Bid Publish Date
28-Dec-2025, 7:48 pm
Bid End Date
13-Jan-2026, 8:00 pm
Location
Progress
Quantity
3000
Bid Type
Two Packet Bid
The State Live Stock Development Department of Chhattisgarh invites procurement for an inactivated rabies veterinary vaccine (cell culture), targeting multiple animal species under government veterinary programs. The contract includes supply of vaccines with primary packaging, specified dosing in vials, and shelf life data. Key differentiators include mandatory licensing from domestic authorities, explicit cold-chain compliance, and requirement to provide all relevant certifications at bid submission. The award will consider adherence to Special Terms and Conditions and the ability to maintain supply at scale, including a potential 25% quantity variation under procurement option clauses. The tender emphasizes regulatory compliance, labeling transparency (virus strain, adjuvants, and administration route), and product approval from the origin country. Location-specific procurement aims to bolster rabies control in the state’s veterinary network.
Vaccine type: Inactivated cell culture rabies vaccine for veterinary use
Labeling: virus strain, adjuvant, route of administration clearly mentioned
Packaging: primary packing type and doses per vial specified
Certifications: BIS licence, type test certificate, ISO 9001 for bidder/OEM
Licensing: valid vaccine manufacturing license under Drugs & Cosmetics Act
Shelf life: defined shelf life at recommended storage temperature
Option clause allows ±25% quantity variation during contract
Bidder must upload BIS/type test/approval certificates with bid
ISO 9001 certification required for bidder or OEM
Not explicitly stated; suppliers should anticipate standard govt terms and ensure invoicing aligned with delivery milestones
Delivery period to commence from order date; option to extend delivery time with extended quantities subject to performance
Not specified; ensure compliance with cold chain, labeling, and timely delivery to avoid potential penalties
ISO 9001 certification for bidder or OEM
BIS licence and type test certificates available
Experience in supplying veterinary vaccines with cold-chain management
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Tender Results
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| Category | Specification | Requirement |
|---|---|---|
| GENERAL | Vaccine name | Rabies Veterinary Vaccine, Inactivated (Cell Culture) |
| GENERAL | Usage | For prophylactic and post-exposure use |
| GENERAL | Targeted species | Dogs, Cattle, Cats |
| PRODUCT INFORMATION | Conformity of Pharmacopoeia | I.P. |
| PRODUCT INFORMATION | Vaccine type | Inactivated (Cell Culture) |
| PRODUCT INFORMATION | Label should contain the virus strain used for preparation and the name of any added adjuvant & route of administration is to be mentioned | Yes |
| PRODUCT INFORMATION | Vaccine Formulation | Liquid |
| PRODUCT INFORMATION | Potency | ≥ 1 IU |
| PRODUCT INFORMATION | Route of Administration | Intramuscular, Subcutaneous |
| PRODUCT INFORMATION | Storage temperature of vaccine | 2 to 8 Degree Celsius |
| PRODUCT INFORMATION | The supply shall be made under proper cold chain conditions | Yes |
| PRODUCT INFORMATION | Compliance to uploaded Special Terms and Conditions | Yes |
| PACKAGING | Primary packing type | Vial |
| PACKAGING | Primary pack size (Number of doses in a vial) | Single Dose, 10 Doses |
| CERTIFICATIONS & REPORTS | Product approved and licensed from the statutory authority in its country of origin | Yes |
| CERTIFICATIONS & REPORTS | Availability of valid vaccine manufacturing license for the product issued from the competent regulatory authority defined under Drugs & Cosmetics Act, 1940 & Rules there under as amended till date | Yes |
| CERTIFICATIONS & REPORTS | Submission of all necessary certifications, licenses and test reports to the buyer at the time of bid submission and/or along with supplies as per buyer requirement | Yes |
| SHELF LIFE | Shelf life of the vaccine from the date of manufacture when stored at recommended temperature | 36 Or higher |
Discover companies most likely to bid on this tender
GST registration certificate
Permanent account number (PAN) card
Experience certificates evidencing vaccine supply capability
Financial statements demonstrating financial stability
EMD/Security deposit document as specified
Technical bid documents showing vaccine specifications
OEM authorization / factory license
BIS licence and type test certificates
Product approvals/licensing from drugs regulatory authority
Extended Deadline
13-Jan-2026, 8:00 pm
Opening Date
13-Jan-2026, 8:30 pm
Extended Deadline
10-Jan-2026, 8:00 pm
Opening Date
10-Jan-2026, 8:30 pm
Key insights about CHHATTISGARH tender market
Bidders must submit BIS licences, type test certificates, and approval certificates alongside ISO 9001 documentation. Include vaccine specifications, cold chain capabilities, and product approvals under the Drugs & Cosmetics Act. Prepare EMD, GST, PAN, and financial statements; ensure labeling includes virus strain and adjuvant details.
Submit GST registration, PAN, experience certificates, financial statements, EMD, BIS/type test certificates, OEM authorization, and product approvals. Provide vaccination label details (virus strain, route, adjuvant) and storage conditions, plus evidence of cold-chain readiness for delivery.
Vaccine type must be inactivated cell culture; potency and storage temperature clearly specified; label includes virus strain and adjuvant; primary packing type and doses per vial must be declared; shelf life at recommended temperature documented.
Eligibility requires ISO 9001 certification, BIS licence and type test certificates, and valid manufacturing licenses under Drugs & Cosmetics Act. Demonstrated capacity to supply veterinary vaccines with cold-chain management and the ability to meet delivery timelines.
Delivery period terms permit extension with the option clause; extension is calculated as (Increased quantity / Original quantity) × Original delivery period, with a minimum of 30 days. Ensure readiness to scale up within 25% variation if invoked.
Labels must show the virus strain, any adjuvant, and route of administration. Primary packing type and the number of doses per vial must be specified, along with storage temperature and cold-chain compliance details.
Upload BIS licence, type test certificate, approval certificates, and other prescribed certificates per Product Specification. Also provide ISO 9001 certification, and country-of-origin vaccine approvals/licensing with bid.
The purchaser may increase/decrease order quantity by up to 25% at contracted rates during/after contract award. Delivery timelines adjust proportionally; bidders should price flexibility into unit costs and confirm storage capacity.
Directorate Of Animal Husbandry
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Main Document
CATALOG Specification
GEM_GENERAL_TERMS_AND_CONDITIONS