General Medicine - Department of Military Affairs - Indian Army
SERTRALINE 50 mg TAB,VENLAFAXINE 37.5 mg TAB,ZOLPIDEM 10 mg TAB,QUETIAPINE 50 mg TAB,TIANEPTINE 12.
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Tender Description
Tender Title: General Medicine
Reference Number: daba1e1e
Issuing Authority: Department of Military Affairs, Ministry of Defence
Scope of Work and Objectives
The General Medicine tender seeks suppliers for an extensive variety of pharmaceuticals crucial for healthcare provisions. This includes a comprehensive array of medications such as SERTRALINE 50 mg, VENLAFAXINE 37.5 mg, ZOLPIDEM 10 mg, QUETIAPINE 50 mg, and TIANEPTINE 12 mg, among others. The primary objective is to procure high-quality medications that meet the rigorous health standards necessary for both military and civilian healthcare needs.
Tender BOQ Items
91 ItemsGeneral Information
Financial Information
Evaluation and Technical Information
Tender Documents
4 DocumentsDocuments Required from Seller
- Experience Criteria
- Past Performance
- Bidder Turnover
- Certificate (Requested in ATC)
- OEM Authorization Certificate
- OEM Annual Turnover
- Compliance of BoQ specification and supporting document *In case any bidder is seeking exemption from Experience / Turnover Criteria
- the supporting documents to prove his eligibility for exemption must be uploaded for evaluation by the buyer
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Frequently Asked Questions
The eligibility requirements include being a registered entity within the pharmaceutical sector, demonstrating compliance with applicable health standards, and possessing necessary certifications that validate your capability. Companies must submit documentation attesting to their eligibility, financial stability, and past performance regarding similar supply contracts.
Bidders must provide essential certificates of compliance with international quality standards governing pharmaceuticals. This typically includes licenses to operate as a pharmaceutical supplier, good manufacturing practices (GMP) certificates, and any other credentials that reflect adherence to national and international regulations.
The registration process involves creating an account on the official tender portal. Once registered, bidders must complete their company profile and upload relevant documents required for the tender submission. The submission and registration must be completed electronically for processing.
Only PDF document formats are accepted for submission of bids and supporting documents. Each document should be clearly labeled and easily accessible to ensure a smooth evaluation process. Bidders should verify that their submissions meet all quality checks before uploading.
The tender offers special provisions to support MSEs and startups, providing them with opportunities to bid competitively. MSEs may receive preferential treatment during the evaluation process, aiming to encourage participation from smaller entities and foster an inclusive tender environment, especially in the realm of pharmaceuticals.
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