Bid Publish Date
20-Mar-2026, 11:10 am
Bid End Date
11-Apr-2026, 5:00 pm
Value
₹1,25,204
Location
Progress
Quantity
22600
Bid Type
Two Packet Bid
The Department of Health and Family Welfare invites bids for the supply of Linezolid 600 mg tablets (anti TB drug) with a total estimated value of ₹125,204.00. Bidders must provide evidence of government/PSU supply experience and comply with bundled documentation, including licenses and certifications. The bid emphasizes full conformity to uploaded technical specifications, labeling, packaging, storage, and logo requirements. Unit packs and country-of-origin approvals are integral, as is the requirement for drug manufacturing licenses valid under the Drugs & Cosmetics Act. This procurement requests a complete supply scope as per the technical specification and includes a Make in India authorization clause, ensuring domestic manufacturing compliance.
Product/service: Linezolid 600 mg tablets (Anti TB drug)
Unit pack size as per technical specification
Labeling, packaging, storage, and logos per uploaded specs
Statutory drug manufacturing license under Drugs & Cosmetics Act
Product approval from origin country statutory authority
Submission of all necessary certifications, licenses, and test reports
Shelf life as specified in technical documentation
Material Test Certificate to accompany supply
Acceptance determined by buyer's lab test results
EMD exemption possible if MSME/NSIC certificate provided
Make in India authorization certificate required
Integrity Pact to be uploaded and signed by bidders
Quantity may vary by up to 50% during contract
Delivery schedule aligned to last/extended delivery orders
Payment terms linked to delivery orders; subject to material test results from buyer's lab before acceptance.
Delivery window extends from last date of original delivery order; extended period affected by option clause with minimum 30 days.
Not explicitly stated; acceptance subject to lab results; potential penalties as per buyer policy after inspection.
Experience certificate for government/PSU/private sector supply
Make in India authorization and valid drug manufacturing license
Integrity Pact compliance and signed submission
Possession of GST registration and PAN, along with financial statements
Tender Category
Goods
Bid To RA
No
Bid To RA Enabled
Yes
Item Category
Anti TB Drugs - Linezolid 600 mg Tablets (Q1)
End-to-end support — bid preparation, GeM registration, document filing & compliance by industry experts.
Free consultation · 24h response
Main Document
CATALOG Specification
TECHNICAL
OTHER
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS
| Category | Specification | Requirement |
|---|---|---|
| PRODUCT INFORMATION | Drug name | Linezolid 600 mg Tablets |
| PRODUCT INFORMATION | Conformity to technical specifications including labeling, packaging, storage, logos etc | As per detailed technical specifications uploaded in GeM Portal |
| PRODUCT INFORMATION | Uploaded technical specification has been seen, read and understood | Yes |
| PRODUCT INFORMATION | Compliance to uploaded Technical Specifications | Yes |
| PRODUCT INFORMATION | Compliance to uploaded Special Terms and Conditions | Yes |
| PRODUCT INFORMATION | Scope of supply covers all components complete as per uploaded techhnical specifications | Yes |
| PRODUCT INFORMATION | Unit pack size | Strip of 10 Tablets |
| CERTIFICATIONS & REPORTS | Product approved from the statutory authority in its country of origin | Yes |
| CERTIFICATIONS & REPORTS | Availability of valid own drug manufacturing license for the product issued from the competent regulatory authority defined under Drugs & Cosmetics Act, 1940 & Rules there under as ammended till date | Yes |
| CERTIFICATIONS & REPORTS | Submission of all necessary certifications, licenses and test reports to the buyer | Yes |
| SHELF LIFE | Shelf life of the drug | As per uploaded Technical Specifications on GeM Portal |
| ADDITIONAL REQUIREMENT | Additional Requirement | NA |
Discover companies most likely to bid on this tender
GST registration certificate
PAN card
Experience certificates for Govt/PSU/private sector supply
Financial statements
EMD/Security deposit documentation (or MSME/NSIC exemption certificate)
Technical bid documents
Manufacturing license under Drugs & Cosmetics Act
Make in India authorization certificate
Integrity Pact signed copy
OEM authorization (if applicable)
Material Test Certificate
Lab test reports from buyer's lab (as applicable)
Extended Deadline
11-Apr-2026, 5:00 pm
Opening Date
11-Apr-2026, 5:30 pm
Key insights about DELHI tender market
Register as a bidder with the health department, submit Experience certificates for govt/PSU supply, provide Make in India authorization, drug manufacturing license under Drugs & Cosmetics Act, and an Integrity Pact. Include GST, PAN, financials, and Material Test Certificate; ensure conformity to uploaded specs.
Required documents include GST registration, PAN, experience certificates for govt/PSU supply, financial statements, EMD proof or MSME/NSIC exemption, technical compliance documents, drug manufacturing license, Make in India authorization, and signed Integrity Pact; also include Material Test Certificate and lab reports as applicable.
Standards mandate conformity to uploaded technical specifications, including labeling, packaging, storage, and logos; product approval from origin country statutory authority; Drugs & Cosmetics Act license; and Material Test Certificate with buyer lab acceptance.
Delivery terms allow an extended period after the last delivery order date; option clause permits up to 50% quantity change with pro-rated delivery time, minimum 30 days; actual schedule will follow contract and PO dates.
If you are not MSME/NSIC exempt, provide EMD as per tender terms; otherwise enclose MSME/NSIC exemption certificate; ensure all EMD-related documentation accompanies the bid submission.
Acceptance is determined by the buyer's lab test results; Material Test Certificate must accompany supply; non-conforming lots may be rejected per buyer’s policy and lab findings.
Mandatory licenses include a valid drug manufacturing license under Drugs & Cosmetics Act and origin-country approval; Make in India authorization and a signed Integrity Pact are also required for bid submission.
Scope covers all components per uploaded technical specifications; unit pack size is defined in the technical docs; ensure full conformity to labeling, packaging, storage, and logo requirements as per uploaded specs.
Sign up now to access all documents
Main Document
CATALOG Specification
TECHNICAL
OTHER
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS