Consumables - Department of Health Research

The eligibility requirements include being a registered entity, compliance with health and safety regulations, and prior experience in supplying medical consumables. Bidders must demonstrate their capability and reliability in delivering diagnostic kits, particularly ELISA kits.

Bidders are required to submit relevant certifications indicating compliance with international standards for medical devices. This includes quality assurance certifications and any specific documentation showing the kits’ validation for clinical use.

The registration process involves submitting comprehensive documentation through the designated procurement portal. Bidders must ensure that all materials are in the required formats and meet the outlined criteria to avoid disqualification from the bidding process.

Bidders are expected to submit a competitive pricing proposal along with an Earnest Money Deposit (EMD), if applicable. Payment terms will be outlined in the tender documents and are typically based on deliverables and acceptance criteria established during the evaluation process.

Yes, this tender includes special provisions that encourage participation from Micro, Small, and Medium Enterprises (MSEs) and startups, promoting local manufacturing and procurement under policies like ‘Make in India’. Benefits may be provided as incentives to foster local entrepreneurship and participation in the health sector supply chain.