Medical Health and Family Welfare Department Uttar Pradesh Dengue Malaria Typhoid Rapid Test Kits Tender 2025
N/a
ETAH, UTTAR PRADESH
Bid Publish Date
05-Jun-2026, 3:50 pm
Bid End Date
15-Jun-2026, 5:00 pm
EMD
₹15,000
Value
₹59,75,000
Location
Progress
Quantity
2600
Category
Point of Care Rapid Test Kits for Humans – Dengue, Malaria, Typhoid & Others
Bid Type
Two Packet Bid
The Regional Institute Of Medical Sciences Imphal Manipur, under the Department Of Health And Family Welfare, invites bids for Point of Care Rapid Test Kits for humans covering Dengue, Malaria, Typhoid and related diseases. Estimated value is ₹5,975,000 with an EMD of ₹15,000. Location: IMPHAL WEST, MANIPUR 795001. Procuring category emphasizes rapid test kits with ISI/MD compliance, packaging that includes positive and negative controls, and tests per pack. Unique factors include mandatory Make in India authorization and experience in supplying to government bodies, with scope for OEM/authorised resellers. This tender emphasizes regulatory compliance and readiness for government health programs.
Product: Point of Care Rapid Test Kits for humans (Dengue, Malaria, Typhoid & others)
Detection type and sample type: specified as product information; exact combinations not disclosed in data
Test per pack: number of tests per pack to be specified in packaging details
Performance metrics: sensitivity and specificity percentages to be provided for each panel
Controls: positive and negative controls included with each pack
Certifications: compliance with Drugs and Cosmetic Act 1940 and MDR 2017; valid Medical Device license required
OEM/Authorization: Make in India authorization and OEM authorization required for bidders; installation by OEM-certified personnel
EMD of ₹15,000; exemptions for MSME/NSIC with certificate
3 years govt/PSU supply experience; primary product value criterion applies
OEM/Make in India authorization and OEM installation/training by certified personnel
Delivery/quantity flexibility up to 50% under option clause; extended delivery terms
GST handling per bidder; integrity pact compliance and End User Certificate if requested
GST payable by bidder; reimbursement as per actuals or applicable rates; no buyer liability for GST calculations
Option to increase/decrease quantity up to 50% at contract placement; delivery period adjustment based on extended quantity
Not explicitly stated; implied LD terms align with standard govt tender practices for delayed delivery
3 years’ experience supplying similar rapid test kits to Central/State Govt/PSU
Demonstrated OEM or authorized distributor authorization with end-user support ability
Not in liquidation or bankrupt; valid GST registration; financial stability evidence
Tender Category
Goods
Bid To RA
No
Bid To RA Enabled
No
Item Category
Point of Care Rapid Test Kits for Humans – Dengue, Malaria, Typhoid & Others (Q2)
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Main Document
CATALOG Specification
CATALOG Specification
CATALOG Specification
OTHER
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS
N/a
ETAH, UTTAR PRADESH
N/a
LUCKNOW, UTTAR PRADESH
Indian Army
CHENNAI, TAMIL NADU
Employees State Insurance Corporation (esic)
KOLLAM, KERALA
Indian Air Force
Tender Results
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| Category | Specification | Requirement |
|---|---|---|
| PRODUCT INFORMATION | Type of Test Kit | Scrub Typhus IgM & IgG Antibody Detection Rapid Test Kit |
| PRODUCT INFORMATION | Detection Type | Qualitative |
| PRODUCT INFORMATION | Sample Type | Serum and Plasma |
| PRODUCT INFORMATION | Result Time | ≤ 15 minutes |
| PRODUCT INFORMATION | Sensitivity (%) | ≥ 99 Or higher |
| PRODUCT INFORMATION | Specificity (%) | ≥ 99 Or higher |
| PRODUCT INFORMATION | Positive and negative controls provided with each pack of kit | Yes, No |
| PACKAGING | Number of Tests per Pack | 25 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 |
Discover companies most likely to bid on this tender
GST registration certificate
PAN card
Experience certificates for supply to Govt/PSU
Financial statements or undertakings showing financial standing
EMD submission document (₹15,000) or MSME/NSIC exemption certificate
Make in India authorization certificate
OEM authorization/certificate if bidding through distributor
Integrity Pact signed copy
End User Certificate format (if requested)
Technical bid documents showing product specs and certifications
Key insights about MANIPUR tender market
Bidders must meet 3-year govt/PSU supply experience, provide OEM/Make in India authorization, and submit EMD of ₹15,000. Include GST details, integrity pact, and End User Certificate if requested. Ensure compliance with Drugs and Cosmetic Act 1940 and MDR 2017 with valid medical device license.
Submit GST registration, PAN, 3-year govt/PSU supply experience certificates, financial statements, EMD documents, OEM authorization, Make in India certificate, and signed integrity pact. End User Certificate format provided by buyer may be required with bid submission.
Kits must provide positive and negative controls per pack; specify sensitivity and specificity percentages for each disease panel; compliant with Drugs and Cosmetic Act 1940 and MDR 2017; must have valid Medical Device license; packaging details include tests per pack.
EMD is ₹15,000. Exemptions possible if bidder provides MSME/NSIC exemption certificate; bidders must still meet experience and licensing requirements and provide Make in India authorization.
Delivery schedule is flexible under the option clause allowing up to 50% quantity variation. Installation/commissioning must be performed by OEM or OEM-certified resources; extended delivery time applies when quantities increase.
Kits must comply with Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017, with a valid Medical Device license from the competent authority; OEM authorization and Make in India certification are required for bidding.
Bidders must provide a Make in India authorization certificate; if bidding through an OEM, include OEM authorization with name, designation, address, email, and phone; installation and after-sales support must be OEM-certified.
End User Certificate may be requested in buyer's standard format; bidders should be prepared to supply the certificate to confirm usage rights and prevent diversion; ensure format compatibility with buyer's requirements.
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Main Document
CATALOG Specification
CATALOG Specification
CATALOG Specification
OTHER
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS