Bid Publish Date
17-Oct-2025, 3:39 pm
Bid End Date
03-Nov-2025, 4:00 pm
Location
Progress
Quantity
799000
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.
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
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 begins after order; option for quantity up to 25% with extended time as per formula; minimum extension time 30 days when applicable.
LD provisions to be invoked for delayed supplies as per contract; specific percentage not disclosed here.
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
Main Document
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS
| 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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Extended Deadline
03-Nov-2025, 4:00 pm
Opening Date
03-Nov-2025, 4:30 pm
Key insights about ANDAMAN & NICOBAR tender market
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.
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.
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.
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.
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.
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.
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Main Document
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
CATALOG Specification
ATC
GEM_GENERAL_TERMS_AND_CONDITIONS