Open Tender for Urea ,R1 5x44ml,R2 5x11ml,Creatinine,R1 5x44ml,R2 5x11ml,LDL R1 2x30ml,R2 2x10ml,T.Bilirubin ,R1 6x

The eligibility requirements include being a registered entity with the necessary industry certifications and demonstrating past performance through relevant contracts. Compliance with OEM authorization and submission of documentation for any exemption claims is also critical.

Bidders should include detailed technical specifications that align with the Bill of Quantities (BoQ) outlined in the tender. This includes compliance certificates, quality standards adherence, and performance documentation for the products offered.

Yes, bidders are required to submit an OEM authorization certificate and documentation demonstrating compliance with all technical specifications and past performance to validate their submission.

Bidders must be registered entities and should ensure they have all necessary certifications and documents in place before attempting to submit a bid. The registration can typically be done through relevant government platforms.

All document submissions must adhere to the formats specified in the tender documents. Typically, formats will include PDF, Word documents, or electronic formats as indicated by the Department of Health Research.

Quality standards must be demonstrated through compliance documentation and certifications provided by the bidder. These should validate the reliability and safety of the consumables being procured.

Bidders must comply with all outlined specifications in the tender documents, including providing necessary documentation and adhering to quality and performance benchmarks as set forth in the BoQ.

Yes, bidders may be required to furnish an EMD based on the value of the bid. This deposit serves to ensure the commitment of bidders to fulfill their obligations if selected.

A performance security will be mandated from successful bidders as a guarantee for the fulfillment of contract terms. The specifics of the amount and conditions will be outlined in the final contractual agreement.

Payment terms will typically be communicated upon selection but may include milestone payments or full payment upon delivery and acceptance of the consumables as per contract stipulations.

Price evaluations will consider not only the bid price but also compliance with technical specifications and quality standards established in the tender. The most advantageous bid based on this evaluation will be selected.

Bidders should submit their documents through the designated platforms as outlined in the tender instructions, ensuring all necessary documents are included and labeled correctly.

While specific dates are not provided, bidders should closely adhere to the submission deadlines stated in the tender, ensuring all required documentation and proposals are submitted within the designated timeframe.

The evaluation process is item-wise, ensuring each bid is thoroughly assessed on technical compliance, financial capability, and overall submission quality, leading to a fair and transparent selection of the winning bidder.

Post-evaluation, bidders will be notified of the results through official communications from the Department of Health Research, including details regarding contract awarding.

MSEs may enjoy benefits such as relaxed eligibility criteria and enhanced support during the bidding process, encouraging diverse and competitive participation in the tender.

Startups may be eligible for similar support provisions as MSEs, including eased qualification criteria and potential networking opportunities to promote successful bid submissions.

The tender encourages local sourcing and stipulations that align with the Make in India initiative, promoting the procurement of products manufactured in India to support local industries.

The tender adheres to local content and procurement rules, supporting the acquisition of consumables from local manufacturers wherever feasible, fostering growth and sustainability within the Indian market.