Point of Care Rapid Test Kits for Humans – Dengue, Malaria, Typhoid & Others
Indian Army
JALANDHAR, PUNJAB
Bid Publish Date
29-Jun-2026, 9:05 am
Bid End Date
09-Jul-2026, 10:00 am
Location
Progress
Quantity
78
Bid Type
Two Packet Bid
The Indian Army, Department Of Military Affairs, invites bids for Point of Care Rapid Test Kits for humans covering Dengue, Malaria, Typhoid and related infections. PROCUREMENT category targets rapid diagnostic kits with defined test counts per pack and validated controls. Key differentiators include compliance with Drugs and Cosmetic Act 1940, Medical Device Rules 2017, and a valid Medical Device license. Bidders must demonstrate 3 years of prior govt supply experience and ISO 9001 certification. The scope emphasizes local servicing via OEM authorization and robust post‑sale support. The opportunity is shaped by strict regulatory alignment and quality control expectations.
Point of Care Rapid Test Kit for humans
Test Kit Type: specified in tender; include positive/negative controls in each pack
Tests per Pack: as per packaging details
Certification: Drugs and Cosmetic Act 1940; MDR 2017 amendments
License: valid Medical Device license issued by competent authority
Quality: ISO 9001 certification; Material Test Certificate with each supply
Documentation: BIS licenses and type test certificates where applicable
EMD: not specified in data; ensure bid documents include bank guarantee if required
Delivery: option to adjust quantity up to 50% at order; extended timelines with minimum 30 days
Eligibility: 3 years govt procurement experience; ISO 9001 certification; OEM authorization
Not disclosed; ensure readiness to comply with standard govt tender payment terms upon award
Delivery period linked to original and extended delivery orders; additional time formula provided (increased quantity/original quantity) × original delivery period with minimum 30 days
Penalties not explicitly stated; ensure understanding from final tender terms before contract
3 years govt or PSU procurement experience for similar rapid test kits
ISO 9001 certification (bidder or OEM)
Manufacturer Authorization if bidding via distributors
Valid Medical Device license for the product
India-based after‑sales support for imported products
Tender Category
Goods
Bid To RA
No
Bid To RA Enabled
Yes
Item Category
Point of Care Rapid Test Kits for Humans – Dengue, Malaria, Typhoid & Others (Q2)
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Main Document
CATALOG Specification
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS
Indian Army
JALANDHAR, PUNJAB
Indian Army
JALANDHAR, PUNJAB
Employees State Insurance Corporation (esic)
SOUTH DELHI, DELHI
Bharat Heavy Electricals Limited (bhel)
HARIDWAR, UTTARAKHAND
Employees State Insurance Corporation (esic)
MUMBAI, MAHARASHTRA
Tender Results
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| Category | Specification | Requirement |
|---|---|---|
| PRODUCT INFORMATION | Type of Test Kit | Cardiac Troponin T Rapid Test Kit |
| PRODUCT INFORMATION | Result Time | ≤ 15 minutes |
| PRODUCT INFORMATION | Positive and negative controls provided with each pack of kit | No |
| 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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Copy of PAN Card
Copy of GSTIN
Copy of Cancelled Cheque
Copy of EFT Mandate certified by Bank
Evidence of 3 years govt supply experience with contracts
OEM Authorization Form / Certificate (if using authorized distributors)
ISO 9001 certification (bidder or OEM)
Material Test Certificate to be sent with supply
BIS licence, type test certificates and other relevant approvals
Evidence of valid Medical Device license for the product
Authorised Seller/OEM registered office details for after‑sales (if imported)
Bidders must submit PAN, GSTIN, cancelled cheque, EFT mandate, and evidence of 3 years govt supply experience. Include ISO 9001 certificates, OEM authorization, and Medical Device license. Ensure compliance with MDR 2017 and Drugs and Cosmetic Act 1940, with Material Test Certificate accompanying delivery.
Required documents include PAN, GSTIN, cancelled cheque, EFT mandate, OEM authorization if using distributors, evidence of 3 years govt supply, ISO 9001 certificate, Material Test Certificate, BIS/type test certificates, and valid Medical Device license for the product.
Bidders must ensure compliance with Drugs and Cosmetic Act 1940, Medical Device Rules 2017, ISO 9001 certification, and where applicable BIS licenses and type test certificates. Imported products need India-based after‑sales support and OEM authorization.
The buyer may adjust quantity up to 50% at contract placement and during currency, with delivery time calculated as (additional quantity/original quantity) × original delivery period, minimum 30 days, and may extend to the original period under option clause.
If bidding via authorized distributors, submit OEM authorization detailing name, designation, address, email, and phone. This ensures post‑sale service and compliance with MDR 2017 and ISO 9001 requirements.
Bidders must provide a valid Medical Device license for the product issued by the competent authority as part of mandatory certifications, enabling marketplace compliance for the rapid test kits.
Nlc India Limited
📍 CUDDALORE, TAMIL NADU
Indian Army
📍 JALANDHAR, PUNJAB
Employees State Insurance Corporation (esic)
📍 MUMBAI, MAHARASHTRA
Surat District Panchayat
📍 SURAT, GUJARAT
N/a
📍 GORAKHPUR, UTTAR PRADESH
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Main Document
CATALOG Specification
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS