GEM

State Livestock Development Department Rabies Veterinary Vaccine Tender Chhattisgarh 2025 - Inactivated (Cell Culture) ISI/ISO 9001

Bid Publish Date

28-Dec-2025, 7:48 pm

Bid End Date

13-Jan-2026, 8:00 pm

Latest Corrigendum Available

Progress

Issue28-Dec-2025, 7:48 pm
Corrigendum10-Jan-2026
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

3000

Bid Type

Two Packet Bid

Key Highlights

  • Exact brand/licensing requirements: BIS licence, type test certificate, and approval certificates
  • Technical standards: ISO 9001 certified supplier or OEM; ISI labeling details
  • Special terms: 25% quantity variation right; extended delivery timelines
  • Critical eligibility: domestic regulatory approvals for vaccines under Drugs & Cosmetics Act
  • Warranty/AMC: Not explicitly stated; ensure compliance with labeling and shelf life
  • Penalties: Liquidated damages not specified; adhere to delivery schedule
  • Delivery: Cold chain maintained; primary packing and vial-dose details required
  • Documentation: Submit all required certificates at bid submission and with supplies

Categories 1

Tender Overview

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.

Technical Specifications & Requirements

  • Vaccine type: Inactivated, cell culture-based rabies vaccine for veterinary use
  • Vaccine formulation and potency: Must specify potency and storage temperature; documented shelf life
  • Labeling/packaging: Label must disclose virus strain, adjuvant details, route of administration, primary packing type, and number of doses per vial
  • Compliance: BIS licence, type test certificates, and any required approvals per Product Specification; ISO 9001 certified OEM or supplier required
  • Certifications/Reports: Valid vaccine manufacturing license under Drugs & Cosmetics Act; submission of tests and licenses at bid and with supplies
  • Cold chain: Proper cold chain infrastructure and documented cold chain maintenance during transport
  • Shelf life: Specify vaccine shelf life from date of manufacture under recommended temperature; ensure compatibility with storage parameters
  • BOQ/Items: No BOQ items listed; ensure supply capacity aligns with demand
  • Delivery: Compliance with delivery timelines and option-based quantity adjustments under contract terms

Terms, Conditions & Eligibility

  • EMD/Security: Provide security as per tender terms; exact amount not listed in data
  • ISO 9001: Bidder or OEM must hold ISO 9001 certification
  • Documentation: Upload BIS licence, type test certificates, approval certificates, and other prescribed certificates at bid
  • Licensing: Availability of product approvals/licensing from domestic regulatory authorities
  • Delivery & Payment: Follow the option clause allowing ±25% quantity changes; ensure delivery in line with extended timelines if exercised
  • Warranty/Compliance: Adhere to special terms; ensure compliance with packaging and labeling requirements as specified
  • Eligibility: Demonstrated capability for veterinary vaccine supply, cold chain management, and regulatory compliance
  • Other: Bidder to comply with all buyer-added terms and conditions; ensure all certificates are current

Key Specifications

  • 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

Terms & Conditions

  • 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

Important Clauses

Payment Terms

Not explicitly stated; suppliers should anticipate standard govt terms and ensure invoicing aligned with delivery milestones

Delivery Schedule

Delivery period to commence from order date; option to extend delivery time with extended quantities subject to performance

Penalties/Liquidated Damages

Not specified; ensure compliance with cold chain, labeling, and timely delivery to avoid potential penalties

Bidder Eligibility

  • 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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Technical Specifications 1 Item

Item #1 Details

View Catalog
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

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Required Documents

1

GST registration certificate

2

Permanent account number (PAN) card

3

Experience certificates evidencing vaccine supply capability

4

Financial statements demonstrating financial stability

5

EMD/Security deposit document as specified

6

Technical bid documents showing vaccine specifications

7

OEM authorization / factory license

8

BIS licence and type test certificates

9

Product approvals/licensing from drugs regulatory authority

Corrigendum Updates

2 Updates
#1

Update

10-Jan-2026

Extended Deadline

13-Jan-2026, 8:00 pm

Opening Date

13-Jan-2026, 8:30 pm

#2

Update

07-Jan-2026

Extended Deadline

10-Jan-2026, 8:00 pm

Opening Date

10-Jan-2026, 8:30 pm

Frequently Asked Questions

Key insights about CHHATTISGARH tender market

How to bid for rabies vaccine tender in Chhattisgarh 2025?

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.

What documents are required for veterinary vaccine procurement in Chhattisgarh?

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.

What are the technical specifications for the rabies vaccine tender in this state?

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.

What is the eligibility criteria for vaccine suppliers in Chhattisgarh?

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.

When is the delivery deadline for the vaccine contract?

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.

What are the labeling and packaging requirements for the vaccine bid?

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.

What certifications must be uploaded with the bid submission?

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.

How does the 25% quantity variation clause affect pricing?

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.

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