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Contract Bidding Open For Rapid Pregnancy Test Kit,Point of Care Rapid Test Kits for Humans – Dengue, Malaria, Typhoid & Ot

Bid Publish Date

09-Jun-2026, 3:17 pm

Bid End Date

20-Jun-2026, 2:00 pm

EMD

₹47,478

Value

₹47,47,780

Progress

Issue09-Jun-2026, 3:17 pm
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

11634

Category

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

Bid Type

Two Packet Bid

Categories 2

N/a invites bids for Rapid Pregnancy Test Kit (Q2), Point of Care Rapid Test Kits for Humans – Dengue, Malaria, Typhoid & Others (Q2), Rapid Test Kit for HIV / Syphilis / Hepatitis B Virus (HBV) / Hepatitis C Virus (HCV) (Q2). Quantity: 11634. Submission Deadline: 20-06-2026 14: 00: 00. Submit your proposal before the deadline.

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

Yes

Item Category

Rapid Pregnancy Test Kit (Q2) , Point of Care Rapid Test Kits for Humans – Dengue, Malaria, Typhoid & Others (Q2) , Rapid Test Kit for HIV / Syphilis / Hepatitis B Virus (HBV) / Hepatitis C Virus (HCV) (Q2)

Authority Records

MEDICAL HEALTH AND FAMILY WELFARE DEPARTMENT

BID & GeM Expert Consultancy

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

Bid Preparation GeM Registration Document Filing

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Documents 9

GeM-Bidding-9387092.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

CATALOG-Specification-2

CATALOG Specification

CATALOG-Specification-3

CATALOG Specification

CATALOG-Specification-4

CATALOG Specification

CATALOG-Specification-5

CATALOG Specification

CATALOG-Specification-6

CATALOG Specification

CATALOG-Specification-7

CATALOG Specification

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

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Closed: 16 April 2026
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Technical Specifications 7 Items

Item #1 Details

View Catalog
Category Specification Requirement
PRODUCT INFORMATION Sample Type Urine
PACKAGING Number of Tests per Pack 10 Tests
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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Historical Data

Required Documents

1

Experience Criteria

2

Past Performance

3

Bidder Turnover

4

Certificate (Requested in ATC)

5

OEM Authorization Certificate

6

OEM Annual Turnover

7

Additional Doc 1 (Requested in ATC)

8

Additional Doc 2 (Requested in ATC) *In case any bidder is seeking exemption from Experience / Turnover Criteria

9

the supporting documents to prove his eligibility for exemption must be uploaded for evaluation by the buyer

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