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Employees State Insurance Corporation HIV/Syphilis/HBV/HCV Rapid Test Kit Tender India 2026

Bid Publish Date

24-Jun-2026, 10:03 am

Bid End Date

04-Jul-2026, 11:00 am

Progress

Issue24-Jun-2026, 10:03 am
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

2

Bid Type

Two Packet Bid

Key Highlights

  • โ€ข Specific brand/OEM requirements for rapid test kits
  • โ€ข MDR 2017 and Drugs and Cosmetic Act compliance mandatory
  • โ€ข Kit insert and controls included with each pack
  • โ€ข Delivery option clause permitting ยฑ25% quantity variation
  • โ€ข 96 tests per contract with defined extension rules
  • โ€ข Evidence of valid Medical Device license required

Categories 2

Tender Overview

Organization: Employees State Insurance Corporation (ESIC) seeks supply of Rapid Test Kits for HIV, Syphilis, HBV, and HCV under a single procurement. Quantity: total tests mandated per contract equals 96 tests, with an option clause allowing quantity variation up to ยฑ25% of bid quantity and during contract currency at contracted rates. Delivery terms: delivery period tied to original delivery date with extension rules stated; minimum added time logic applies. The product must include a kit insert and come with positive/negative controls in each pack. Location details are not disclosed in the available data and appear to be centralized under ESIC procurement. This tender emphasizes regulatory compliance, packaging, and performance verification as differentiators.

Technical Specifications & Requirements

  • Product category: Rapid HIV/Syphilis/HBV/HCV test kits
  • Testing method: Point-of-care immunochromatographic or equivalent rapid assay
  • Detection type: Qualitative positive/negative results
  • Result time: Within manufacturer-stated timeframe
  • Sensitivity/Specificity: Must meet or exceed stated performance in product insert; exact percentages to be provided by bidder
  • Controls: Positive and negative controls included with each kit pack
  • Packaging: Number of tests per pack aligned with kit design; include kit insert
  • Shelf life/Residual shelf life: Must be adequate for intended distribution and storage conditions
  • Certifications: Compliance with Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017 as amended; valid Medical Device license from competent authority required
  • OEM/license: Availability of valid Medical Device license holder or authorized distributor with proof
  • Delivery/installation: Procurement requires timely delivery per option clause; binding delivery schedules to original order and any extended period calculations

Terms, Conditions & Eligibility

  • EMD/Deposit: Not disclosed in the available data; bidders should expect standard ESIC EMD norms per tender terms
  • Experience/Turnover: Prior experience in supplying rapid diagnostic kits and compliance with MDR 2017; turnover thresholds are not specified in available data
  • Payment terms: Not specified in the data; bidders should anticipate ESIC standard payment within a defined period post-delivery
  • Documents: Kit insert included; OEM authorization or distributor proof required; GST and PAN details likely required
  • Option clause: Quantity may be increased or decreased by up to 25%; extended delivery time formula applies
  • Penalties/Warranty: Not specified; standard vendor performance and post-sale support likely applicable
  • Delivery timeline: Delivery commencement from order date; extension rules apply under option clause

Key Specifications

  • Rapid test kit for HIV, Syphilis, HBV, HCV

  • 96 tests per contract

  • Positive/negative controls within packs

  • IS 194/ MDR 2017 compliance

  • Valid Medical Device license from competent authority

Terms & Conditions

  • Option clause allows ยฑ25% quantity change

  • Delivery time to be recalculated for extensions

  • Kit insert and controls required with each pack

Important Clauses

Delivery Terms

Delivery period starts from order date; extended delivery time formula applies for increased quantities; minimum 30 days

Compliance

Products must comply with Drugs and Cosmetic Act 1940 and MDR 2017; valid Medical Device license required

Quantity Variation

Purchaser may increase/decrease quantity by up to 25% during contract and currency

Bidder Eligibility

  • Experience in supplying rapid diagnostic test kits to public entities

  • MDR 2017 and Drugs & Cosmetic Act compliance

  • Valid Medical Device license and OEM authorization

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

Yes

Item Category

Rapid Test Kit for HIV / Syphilis / Hepatitis B Virus (HBV) / Hepatitis C Virus (HCV) (Q2)

Authority Records

MINISTRY OF LABOUR AND EMPLOYMENT

BID & GeM Expert Consultancy

End-to-end support โ€” bid preparation, GeM registration, document filing & compliance by industry experts.

Bid Preparation GeM Registration Document Filing

Free consultation ยท 24h response

Documents 3

GeM-Bidding-9512148.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

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Technical Specifications 1 Item

Item #1 Details

View Catalog
Category Specification Requirement
PRODUCT INFORMATION Type of Test Kit HIV1 & HIV2 Antibodies and HIV1 p24 Antigen Detection Rapid Test Kit
PRODUCT INFORMATION Detection Type Qualitative
PRODUCT INFORMATION Testing Method Flow-Through (Immunoconcentration)
PRODUCT INFORMATION Result Time โ‰ค 15 minutes
PRODUCT INFORMATION Sensitivity (%) โ‰ฅ99%, 100% Or higher
PRODUCT INFORMATION Specificity (%) โ‰ฅ99% Or higher
PRODUCT INFORMATION Positive and negative controls provided with each pack of kit No
PACKAGING Number of Tests per Pack 10 Tests, 20 Tests, 25 Tests, 30 Tests, 40 Tests, 50 Tests, 96 Tests, 100 Tests
SHELF LIFE Residual shelf life of the product Agree to provide residual shelf life of atleast 75% of total shelf life at the time of delivery to the consignee
CERTIFICATIONS Compliance to Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017 as amended till date Yes
CERTIFICATIONS Availability of valid Medical Device license for the product issued from the competent authority Yes

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Required Documents

1

GST certificate

2

PAN card

3

Experience certificates for rapid test kit supply

4

Financial statements

5

EMD/Security deposit details (as per tender norms)

6

Technical bid documents

7

OEM authorizations or distributor agreements

8

Kit insert copies and MDR/Medical Device licenses

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