Department of Health and Family Welfare Tenders (GEM/2025/B/6139035)
Cap Deferiprone 500mg,Cap Danazol 200 mg,Cap Nifedepine 5mg SL,Tab Ascorbic acid 200mg plus Sod Asc

Tender Timeline
Tender Title: Tablets Supply
Reference Number: GEM/2025/B/6139035
Issuing Authority: Department of Health and Family Welfare, Ministry of Health and Family Welfare
The Tablets Supply tender (GEM/2025/B/6139035) is a significant opportunity issued by the Department of Health and Family Welfare under the Ministry of Health and Family Welfare. The scope of work encompasses the supply of various pharmaceutical preparations, particularly focusing on the following:
- Cap Deferiprone 500mg
- Cap Danazol 200mg
- Cap Nifedepine 5mg SL
- Tab Ascorbic acid 200mg plus Sod Asc
Scope of Work and Objectives
The primary objective of this tender is to procure a total quantity of 282,167 units of the specified pharmaceutical products. This initiative aims to ensure the availability of essential medications in healthcare facilities across the country, supporting public health initiatives and enhancing patient care.
Eligibility Criteria
To participate in this tender, bidders must demonstrate compliance with specific eligibility criteria. Bidders are required to be registered entities in accordance with relevant regulatory bodies. Additionally, they must showcase experience in supplying related pharmaceutical products to governmental or healthcare institutions.
Technical Requirements
Participants must meet defined technical requirements including but not limited to:
- Compliance with GMP (Good Manufacturing Practice) standards.
- Adherence to applicable quality standards for pharmaceutical products.
- Provision of necessary certifications indicating the safe and effective manufacturing of medicines.
Financial Requirements
All bidders should possess the financial capability to handle contracts of this magnitude. Financial statements indicating liquidity and operational stability for the preceding fiscal year are required as part of the submission.
Document Submission Details
Bidders must ensure that all required documentation is submitted in compliance with the tender guidelines. Accepted document formats include PDF and Word. Detailed submission instructions are outlined in the tender documents to facilitate a smooth application process.
Special Provisions
As part of the government's initiative to boost Micro, Small, and Medium Enterprises (MSEs) and support startups, there are provisions in place favoring participation from these entities. This includes potential relaxation of certain requirements, thereby encouraging a broader range of competition.
Evaluation Process
The evaluation process will assess bids based on predetermined criteria, including price, quality, compliance with specifications, and the vendor’s past performance. Bidders are encouraged to focus on providing comprehensive details to enhance their evaluation score.
Delivery Locations
The successful bidder(s) will be required to deliver the products to specified healthcare institutions across various locations as indicated in the tender documentation. Timely delivery will be critical to ensure that there are no disruptions in the availability of essential medications.
Contact Information
For any inquiries regarding the tender, contact information is available in the official tender documents. Bidders are encouraged to seek clarification on any points before submitting their proposals.
For more information on the Tablets Supply tender (GEM/2025/B/6139035), and to view the complete requirements and provisions, please refer to the detailed tender documentation provided.
General Information
Financial Information
Evaluation and Technical Information
Tender Documents
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Frequently Asked Questions
The eligibility requirements include being a registered entity compliant with local regulations, possessing prior experience in supplying pharmaceutical products, and capacity to adhere to operational guidelines set by the Ministry of Health and Family Welfare.
Bidders must submit various certificates including ISO certification, GMP compliance certificate, and any other specific regulatory documents that validate their capability to manufacture or supply pharmaceutical products.
The registration process typically involves submitting necessary company information, proof of tax compliance, and adherence to any pre-qualification requirements as specified in the tender documents. It is important to follow the submission guidelines closely.
All documentation should be submitted in PDF or Word format. This includes technical proposals, financial documents, and any essential certificates stated in the tender requirements. Ensure that the submission is complete and adheres to the specified formats.
The evaluation and selection process will assess proposals based on compliance with technical, financial, and regulatory criteria, as well as the competitive pricing offered. Emphasis will be placed on quality certifications and the supplier’s past performance track record.
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