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GEM

Directorate of Health Services Medicine Procurement Tender 2025 Directorate of Health Services - Pharmaceutical Products & Packaging Compliance

Bid Publish Date

17-Oct-2025, 3:39 pm

Bid End Date

03-Nov-2025, 4:00 pm

Latest Corrigendum Available

Progress

Issue17-Oct-2025, 3:39 pm
Corrigendum27-Oct-2025
AwardPending
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Quantity

799000

Categories 9

Tender Overview

The prospective bidder should note that the tender targets the supply of pharmaceutical products under the Directorate of Health Services. The procurement focuses on medicines including details such as medicine name, dosage form, strength, primary packaging type, and pack size. An emphasis exists on valid drug manufacturing licenses, compliance with uploaded special terms, and shelf life from the date of manufacture. The contract includes requirements for submission-ready certifications and test reports, with a scope limited to the supply of goods and potential option clauses for quantity adjustments up to 25%. The bidding framework includes OEM authorization where applicable and a clear adherence to buyer-specified terms. The opportunity is positioned to support government health initiatives with attention to packaging standards and regulatory compliance.

Technical Specifications & Requirements

  • Medicine Name, Dosage Form, Strength: alignment with supplied records and drug regulatory standards.
  • Compliance to uploaded Special Terms and Conditions: bidders must confirm conformance to buyer-stipulated terms.
  • Type of primary packing: specification for blister/strip or bottle packaging as per tender items.
  • Primary pack size: exact number of tablets per strip/blister or per bottle.
  • Validity/licensing: valid drug manufacturing license under the Drugs and Cosmetic Act and Rules, current to date.
  • Certifications & test reports: submission of all required licenses, certifications, and test data at bid submission and with supplies.
  • Shelf life: reported in months from the manufacture date to ensure product viability during distribution.
  • BOQ & scope: no BOQ items listed; scope is limited to the supply of goods with potential extension under option clause.
  • Vendor qualifications: OEM authorizations and material test certificates where required.

Terms, Conditions & Eligibility

  • EMD: required per bid document; submission via approved mode with proof.
  • Delivery & scope: supply-only contract; no installation services implied.
  • Manufacturer authorization: include OEM authorization/certification for authorized distributors.
  • Certificate submission: mandatory certificates, licenses, and test reports with bid and on delivery.
  • Material test certificate: must accompany supplies; buyer lab results are final for acceptance.
  • Bid security options: EMD via DD or fixed deposit receipt; hard copies to be delivered within 5 days of bid end/open date.
  • Performance security: acceptable FDR options; PBG may be required.
  • Option clause: quantity may vary by ±25% with adjusted delivery timelines as defined by the contract terms.

Terms & Conditions

  • Key Term 1: EMD required via DD/FDR and supporting proof with bid submission

  • Key Term 2: OEM authorization required for authorized distributors

  • Key Term 3: Material test certificates mandatory with bid and on delivery

  • Key Term 4: Shelf life specified in months from manufacture date

  • Key Term 5: Quantity may increase up to 25% during contract and currency

  • Key Term 6: Delivery schedule based on last date of original delivery order

Important Clauses

Payment Terms

Bid price must cover all costs; no separate installation charges; EMD and performance security as per terms; payment terms to be defined in contract.

Delivery Schedule

Delivery begins after order; option for quantity up to 25% with extended time as per formula; minimum extension time 30 days when applicable.

Penalties/Liquidated Damages

LD provisions to be invoked for delayed supplies as per contract; specific percentage not disclosed here.

Bidder Eligibility

  • Eligibility for supply of pharmaceutical goods under Drugs and Cosmetic Act

  • Valid drug manufacturing license current to date

  • OEM authorization for required medicines and packaging

Documents 16

GeM-Bidding-8423852.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

CATALOG-Specification-2

CATALOG Specification

CATALOG-Specification-3

CATALOG Specification

CATALOG-Specification-4

CATALOG Specification

CATALOG-Specification-5

CATALOG Specification

CATALOG-Specification-6

CATALOG Specification

CATALOG-Specification-7

CATALOG Specification

CATALOG-Specification-8

CATALOG Specification

CATALOG-Specification-9

CATALOG Specification

CATALOG-Specification-10

CATALOG Specification

CATALOG-Specification-11

CATALOG Specification

CATALOG-Specification-12

CATALOG Specification

CATALOG-Specification-13

CATALOG Specification

Buyer uploaded ATC document

ATC

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

Technical Specifications 13 Items

Item #1 Details

View Catalog
Category Specification Requirement
PRODUCT INFORMATION Medicine Name Acyclovir
PRODUCT INFORMATION Dosage Form Tablet
PRODUCT INFORMATION Strength 400 mg
PRODUCT INFORMATION Compliance to uploaded Special Terms and Conditions Yes
PACKAGING Type of primary packing Strip, Blister
PACKAGING Primary pack size (Number of tablets per strip/blister) 5, 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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Corrigendum Updates

1 Update
#1

Update

27-Oct-2025

Extended Deadline

03-Nov-2025, 4:00 pm

Opening Date

03-Nov-2025, 4:30 pm

Frequently Asked Questions

Key insights about ANDAMAN & NICOBAR tender market

How to bid for medicines tender in Directorate of Health Services 2025

Bidders must submit a complete bid with GST, PAN, experience certificates, financial statements, EMD via DD or FDR, OEM authorization, and material test certificates. Ensure compliance with Drugs and Cosmetic Act licenses and provide shelf-life data from manufacture date.

What documents are required for pharmaceutical tender participation 2025

Required documents include GST registration, PAN card, valid drug manufacturing license, OEM authorization, experience certificates for similar supply, material test certificates, and tender-specific certifications. Upload these with bid and attach hard copies within 5 days after bid end date.

What are the packaging specifications for medicines in this tender

Packaging details specify type of primary packing (blister/strip or bottle) and the exact primary pack size per item. Suppliers must confirm packaging format in their bid and ensure compatibility with shelf-life and regulatory packaging standards.

What is the shelf life requirement for medicines in this bid

Shelf life must be stated in months from the date of manufacture. Bidders should guarantee minimum shelf life at delivery and provide explicit shelf-life data in their technical bid to avoid rejection.

What are the EMD submission requirements for the health medicines tender

EMD must be submitted as a Demand Draft or Fixed Deposit Receipt in favor of the designated authority, with scanned proof uploaded and hard copy delivered within 5 days post bid end date. Ensure correct beneficiary and amount as per tender value.

What certifications are mandatory for bid submission in health services medicines

Mandatory certifications include current drug manufacturing license, OEM authorization, and material test certificates. All documents must be uploaded with the bid and provided again with the supplies per buyer requirements.