GEM

GEM Central Delhi Medicine Supply Tender 2025 – IS 550 drug packaging, DC Act license, MSME NSIC relief

Bid Publish Date

27-Dec-2025, 10:25 am

Bid End Date

12-Jan-2026, 11:00 am

Progress

Issue27-Dec-2025, 10:25 am
AwardPending
Explore all 3 tabs to view complete tender details

Quantity

36000

Categories 2

Tender Overview

The Government e-Marketplace (GEM) tender in CENTRAL DELHI, DELHI seeks vendors for Medicine Name with defined Dosage Form and Strength, including related packaging and regulatory documentation. The bid requires a valid drug manufacturing license under the Drugs and Cosmetics Act, along with submission of all necessary certifications and test reports. Tender scope includes details on the type of primary packing and its primary pack size, and mandates adherence to uploaded Special Terms and Conditions. An integrity pact is mandatory, with MSME/NSIC exemptions possible if applicable. The purchaser reserves rights on quantity variation up to 50%, at contracted rates, and delivery timing linked to original delivery periods. Unique criteria include a Material Test Certificate to accompany supplies.

Technical Specifications & Requirements

  • Medicine Name, Dosage Form, and Strength as specified in the tender document
  • Compliance with uploaded Special Terms and Conditions
  • Packaging: Type of primary packing, Primary pack size (number of tablets per pack)
  • Certifications: Valid drug manufacturing license under Drugs and Cosmetics Act; submission of licenses and test reports with bid and with supplies
  • Shelf Life: Shelf life in months from the date of manufacture
  • Documentation must include integrity pact, Make in India authorization, and supply chain certifications if applicable

Terms, Conditions & Eligibility

  • EMD and/or exemption based on MSME/NSIC as per eligibility criteria
  • Compliance with Integrity Pact and upload of signed copy
  • Include Make in India authorization certificate
  • Option clause allows up to 50% quantity variation during contract
  • Material Test Certificate to be submitted with supply and used as acceptance criterion by Buyer lab

Key Specifications

    • Medicine Name, Dosage Form, and Strength as per BOQ/BOQ-like submission
    • Primary packing: Type and Primary pack size (number of tablets per pack)
    • Shelf life: months from date of manufacture
    • Certifications: Valid drug manufacturing license under Drugs and Cosmetics Act; all test reports required at bid submission and with supplies
    • Compliance with uploaded Special Terms and Conditions; integrity pact
    • Delivery & testing: Material Test Certificate to be used as sole acceptance criterion by Buyer’s Lab

Terms & Conditions

  • EMD to be furnished or exempted per MSME/NSIC eligibility

  • 50% quantity variation allowed during both initial and extended delivery periods

  • Make in India authorization required; signed Integrity Pact to be uploaded

  • Material Test Certificate mandatory with supply and as a quality acceptance criterion

Important Clauses

Payment Terms

Not specified in data

Delivery Schedule

Delivery period linked to original order; option to extend as per 50% quantity variation with minimum 30 days when applicable

Penalties/Liquidated Damages

Not specified in data

Bidder Eligibility

  • Experience certificate for supply to Govt/PSU or reputed private organisations

  • MSME/NSIC exemption certificate (if applicable)

  • Make in India authorization

  • Signed Integrity Pact and compliance with buyer terms

  • Drug manufacturing license under Drugs and Cosmetics Act and related test reports

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Technical Specifications 1 Item

Item #1 Details

View Catalog
Category Specification Requirement
PRODUCT INFORMATION Medicine Name Phenobarbitone
PRODUCT INFORMATION Dosage Form Tablet
PRODUCT INFORMATION Strength 60 mg
PRODUCT INFORMATION Compliance to uploaded Special Terms and Conditions Yes
PACKAGING Type of primary packing Strip
PACKAGING Primary pack size (Number of tablets in a primary pack) 10
CERTIFICATIONS & REPORTS Availability of valid drug manufacturing license issued from the competent authority defined under Drugs and Cosmetic Act and Rules there under as amended till date Yes
CERTIFICATIONS & REPORTS Submission of all necessary certifications, licenses and test reports to the buyer as per buyer requirement at the time of bid submission and along with supplies Yes
SHELF LIFE Shelf life in months from the date of manufacture 24, 36 Or higher

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Required Documents

1

GST certificate

2

PAN card

3

Experience certificates for similar Govt/PSU/private supply

4

Financial statements / turnover evidence

5

EMD document or exemption certificate (MSME/NSIC)

6

Drug manufacturing license under Drugs and Cosmetics Act

7

OEM authorizations (if applicable)

8

Technical bid documents and compliance certificates

9

Integrity Pact signed copy

10

Make in India authorization certificate

11

Material Test Certificate to accompany supplies

Frequently Asked Questions

Key insights about DELHI tender market

How to bid in GEM medicine tender in Central Delhi 2025?

Bidders must meet the eligibility criteria, submit GST, PAN, experience certificates, financials, EMD or MSME exemption, Drug manufacturing license under Drugs and Cosmetics Act, Make in India authorization, and signed Integrity Pact. Include Material Test Certificate with bid and with deliveries, and ensure compliance with Special Terms.

What documents are required for the central delhi medicine tender 2025?

Required documents include GST certificate, PAN, experience certificates for Govt/PSU supply, financial statements, EMD or exemption, Drug manufacturing license under Drugs and Cosmetics Act, OEM authorizations (if applicable), Make in India authorization, Integrity Pact, and Material Test Certificate to accompany supplies.

What are the packaging and shelf life requirements for the medicine tender?

Tender specifies type of primary packing and primary pack size (tablets per pack), along with shelf life in months from the manufacture date. Compliance with packaging terms and testing certificates is required for acceptance by the buyer's lab.

What is the Make in India authorization requirement for bid submission?

Bidders must include Make in India authorization certificate as part of the bid submission and ensure products and manufacturing processes comply with Make in India guidelines, enabling eligibility for the procurement by GEM.

What is the quantity variation clause for this medicine tender?

The purchaser may increase or decrease quantity up to 50% of the bid quantity at contract placement and during currency, with delivery time adjusted accordingly based on the extended period formula.

What are the acceptance criteria related to Material Test Certificate?

Material Test Certificate accompanies each supply; the buyer’s lab will evaluate results, and lab outcomes will be the sole basis for acceptance, making MTCs essential for compliance and payment eligibility.

What standards and licenses must be submitted for drug procurement in Delhi?

Submit a valid Drug Manufacturing License under the Drugs and Cosmetics Act, relevant test reports, and ensure compliance with the uploaded Special Terms. ISI/IS standards or additional certifications may be required per buyer terms.

What is the deadline to submit bids for the central delhi medicine tender?

Bid submission deadlines are defined by GEM portal timelines. Ensure submission of all mandatory documents, Integrity Pact, and MTCs well before the closing time to avoid rejection and ensure eligibility for evaluation.

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