Indian Army Veterinary Medicines Tender Pune Maharashtra 2026 – Fluralaner 1000 mg & Injections with 25% Option Clause

Bidders should ensure registration with the government portal, submit GST and PAN, provide experience certificates for veterinary supply, and attach OEM authorizations if required. The tender outlines a 25% quantity variation right and a delivery-time formula; ensure pricing aligns with contracted rates and prepare for potential quantity changes.

Required documents include GST certificate, PAN card, experience certificates for veterinary supplies, financial statements, EMD documents if applicable, technical bid documents, and OEM authorizations. Prepare product specifications for Tab Fluralaner 1000 mg chewable and the listed injectables.

Delivery starts from the last date of the original delivery order; a 25% quantity option exists during contract and currency. The minimum extended delivery time is 30 days; penalties or LD details are not specified—confirm during bid submission.

The scope covers Tab Fluralaner 1000 mg chewable tablets for 20–40 kg dogs, and injectables Sodium bicarbonate 25 ml, Ranitidine 30 ml, Ethamsylate 100 ml, and Sterilium 500 ml. No additional items are listed in the BOQ.

No explicit standards (e.g., ISO/ISI) are mentioned in the available tender text. Vendors should verify required certifications during bid clarification and align dossier with general government veterinary procurement norms.

Closing dates are not disclosed in the provided data. Bidders should monitor the official government portal, ensure compliance with the option clause, and prepare all mandatory documents to respond promptly when the portal announces deadlines.

Eligibility typically includes registered business, GST, prior supply experience in veterinary/medical sectors, and financial stability. This tender requires adherence to quantity variation rights and delivery-time rules; bidders should ensure capability to flexibly adjust quantities within 25% of bid values.

Check for OEM authorization or authorized distributor certificates in the submission package. If not mandated in reserved terms, include any available supplier authorization to demonstrate product provenance for Tab Fluralaner and listed injectables.