BOQ bid for 8 different kit - Department of Health Research

Western Blot test for detection of HIV1 and HIV2 antibody,Treponema Palladium Hemagglutination Assa

Goods
Qty:1,533

Tender Timeline

Tender Issue
May 29, 2025 at 10:39 AM

Tender Description

Tender Title: BOQ bid for 8 different kit

Tender Reference Number: fa60d2ee
Issuing Authority: Department of Health Research, Ministry of Health and Family Welfare

Scope of Work and Objectives

The objective of this tender is to procure essential testing kits necessary for the detection of HIV1 and HIV2 antibodies as well as the Treponema Pallidum Hemagglutination Assay. The proposed purchase will include a total of 1,533 units distributed across different kits, ensuring that healthcare facilities have access to necessary diagnostics for better management of public health.

Tender BOQ Items

8 Items
1.

Western Blot test for detection of HIV1 and HIV2 antibody

Western Blot test for detection of HIV1 and HIV2 antibody detailed specifications mentioned in specification document

Qty:4
Unit:kit
480
2.

Treponema Palladium Hemagglutination Assay

Treponema Palladium Hemagglutination Assay (TPHA) detailed specifications mentioned in specification document

Qty:1200
Unit:test
450
3.

Multi check CD4 Low Control Kit

Multi check CD4 Low Control Kit detailed specifications mentioned in specification document

Qty:18
Unit:vial
540
4.

Real-Time Chlamydia trachomatis and Neisseria gonorrhoeae PCR detection kit

Real-Time Chlamydia trachomatis and Neisseria gonorrhoeae PCR detection kit detailed specifications mentioned in specification document

Qty:4
Unit:kit
450
5.

Chlamydia trachomatis antigen detection kit

Chlamydia trachomatis antigen detection kit detailed specifications mentioned in specification document

Qty:300
Unit:test
450
6.

Chlamydia trachomatis IgG antibody detection ELISA kit

Chlamydia trachomatis IgG antibody detection ELISA kit detailed specifications mentioned in specification document

Qty:3
Unit:kit
365
7.

Elisa kit for quantitative determination of human IL-10 concentrations

Elisa kit for quantitative determination of human IL-10 concentrations detailed specifications mentioned in specification document

Qty:2
Unit:kit
365
8.

Elisa kit for quantitative determination of human IL-17A concentrations

Elisa kit for quantitative determination of human IL-17A concentrations detailed specifications mentioned in specification document

Qty:2
Unit:kit
365

General Information

Item Category
Western Blot test for detection of HIV1 and HIV2 antibody , Treponema Palladium Hemagglutination Assay , Multi check CD4 Low Control Kit , Real-Time Chlamydia trachomatis and Neisseria gonorrhoeae PCR detection kit , Chlamydia trachomatis antigen detection kit , Chlamydia trachomatis IgG antibody detection ELISA kit , Elisa kit for quantitative determination of human IL-10 concentrations , Elisa kit for quantitative determination of human IL-17A concentrations
Organisation Name
State

Financial Information

Bid Offer Validity
180 (Days)
Arbitration Clause
No
Mediation Clause
No

Evaluation and Technical Information

Evaluation Method
Item wise evaluation/
Inspection Required
Yes
Technical Clarifications Time
3 Days

Tender Documents

4 Documents
GeM-Bidding-7900187.pdfMain Document
BOQ DocumentBOQ BOQ
BOQ DocumentBOQ BOQ
GEM General Terms and Conditions DocumentGEM_GENERAL_TERMS_AND_CONDITIONS

Documents Required from Seller

  • Certificate (Requested in ATC)
  • OEM Authorization Certificate
  • Compliance of BoQ specification and supporting document *In case any bidder is seeking exemption from Experience / Turnover Criteria
  • the supporting documents to prove his eligibility for exemption must be uploaded for evaluation by the buyer

Frequently Asked Questions

The eligibility requirements include being a registered entity within the medical supplies domain and possessing valid certifications. Bidders should demonstrate previous experience in supplying similar medical diagnostics, thus ensuring their capability to deliver high-quality products under this tender.

The technical specifications for the kits require adherence to rigorous healthcare protocols, with all products needing FDA or equivalent certifications. Bidders are mandated to provide documents that validate the performance metrics and quality standards aligned with the required testing criteria, ensuring reliability in results.

The Earnest Money Deposit (EMD) is a security measure that all bidders must submit. It serves to authenticate the seriousness of the bid and will be detailed in the tender documents. Failure to provide the EMD can result in disqualification from the bidding process.

The evaluation process involves a multi-faceted approach encompassing both technical compliance and financial analysis. Each proposal will be assessed based on the quality of submitted documentation, adherence to technical specifications, and price evaluation considerations, facilitating an equitable selection outcome.

Yes, the tender provides specific benefits for Micro, Small, and Medium Enterprises (MSEs), including reduced documentation requirements and expedited evaluation processes. This encourages inclusivity and participation from smaller suppliers, thus fostering a diverse procurement landscape.

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