Point of Care Rapid Test Kits for Humans – Dengue, Malaria, Typhoid & Others
Employees State Insurance Corporation (esic)
SOUTH DELHI, DELHI
Bid Publish Date
06-Jul-2026, 10:05 am
Bid End Date
17-Jul-2026, 10:00 am
Location
Progress
Quantity
800
Bid Type
Two Packet Bid
The Department Of Health And Family Welfare seeks Point of Care rapid test kits for humans addressing Dengue, Malaria, Typhoid and related conditions. The scope emphasizes rapid results with specified test types and pack-level controls; each kit must include positive and negative controls. Compliance with the Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017 is mandatory, along with a valid Medical Device license. Offers should reflect recognition of Make in India and MSME/NSIC exemptions if applicable, with an integrity pact signed. The procurement may require product samples before award and adherence to stringent hospital quality checks at PGI Hospital, New Delhi. Key differentiators include certification alignment, regulatory licenses, and supplier credibility demonstrated via experience documents.
Product: Point of Care rapid test kit for Dengue, Malaria, Typhoid
Test kit must include: positive and negative controls
Packaging: specify tests per pack (not given in BOQ)
Certifications: Drugs and Cosmetic Act 1940 compliance; MDR 2017 compliance
Regulatory: valid Medical Device license from competent authority
Delivery/testing: pre-bid sample submission required (2 nos.) at PGI New Delhi
Brand/OEM: Make in India authorisation certificate required if applicable
EMD exemption possible for MSME/NSIC with certificate
Integrity Pact mandatory; bidder to sign and submit
Delivery quantity can vary up to 50% during contract
Two sample units must be submitted before bid end date
Not specified in data; typically subject to delivery milestones and acceptance
Delivery period may adjust with option clause; minimum 30 days for extended delivery
Not specified; standard hospital procurement penalties may apply for non-compliance
Experience certificate for government/private supply with POs
Make in India authorisation
MSME/NSIC exemption (if applicable)
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)
Max Delivery Days
400
Delivery Locations
1
Delivery Cities
New Delhi
Delivery Pincodes
110001
| Consignee | Address | City | State | Pincode | Quantity | Delivery Days | Additional Requirement |
|---|---|---|---|---|---|---|---|
| Vivek | 110001,dr. ram manohar lohia hospital baba kharak singh marg new delhi | New Delhi | Delhi | 110001 | - | 400 | - |
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Main Document
GEM_CATEGORY_SPECIFICATION
OTHER
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS
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BANGALORE, KARNATAKA
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JALANDHAR, PUNJAB
Tender Results
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| Category | Specification | Requirement |
|---|---|---|
| PRODUCT INFORMATION | Type of Test Kit | Cardiac Troponin I Rapid Test Kit |
| PRODUCT INFORMATION | Result Time | ≤ 15 minutes |
| PRODUCT INFORMATION | Positive and negative controls provided with each pack of kit | Yes |
| 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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GST certificate
PAN card
Experience certificates for government/private supply
Financial statements
EMD/Security deposit details
Technical bid documents
OEM authorisations (Make in India, etc.)
Integrity Pact signed copy
Medical Device license validity proof
Key insights about DELHI tender market
Bidders must submit GST, PAN, experience certificates, financials, EMD, technical bid, OEM authorisations, and an Integrity Pact. Compliance with MDR 2017 and Drugs and Cosmetic Act is mandatory. Prepare 2 sample units for pre-bid evaluation at PGI New Delhi two days before bid end date.
Required documents include GST certificate, PAN, government/private experience certificates with PO references, financial statements, EMD receipts, technical compliance certificates, OEM authorisations, and signed Integrity Pact. Make in India authorization may be necessary for eligibility.
Kits must comply with Drugs and Cosmetic Act 1940 and MDR 2017, with a valid Medical Device license from the competent authority. Evidence of these certifications should accompany the bid submission.
Delivery time extends by (Increased quantity ÷ Original quantity) × Original delivery period, with a minimum of 30 days. The purchaser may extend up to the original delivery period while exercising the option clause.
Submit 2 sample units at Procurement Section, 4th Floor, PGI Building, Dr. Ram Manohar Lohia Hospital, New Delhi, at least two days before bid end date. Include bid number, item number, and bidder details clearly.
Yes, if the bidder holds MSME/NSIC registration, attach the EMD exemption certificate. Ensure the certificate is valid and accompanies the bid package for eligibility evaluation.
Provide Make in India authorisation certificate as part of the technical bid to demonstrate local manufacturing capability, supporting regulatory compliance and faster procurement processing.
Demonstrate prior government/private supply experience with POs, possess a valid Medical Device license, submit OEM authorisations, and sign the Integrity Pact. Achieve MDR 2017 compliance and provide 2 pre-bid samples for evaluation.
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Main Document
GEM_CATEGORY_SPECIFICATION
OTHER
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS