Drugs and Pharmaceutical Products
Amlodipine besylate 5 mg Tab,Linezolid 600mg Tab,Clarithromycin 500mg Tab,Inj Teriparatide 750 mcg
Tender Timeline
Tender Title: Drugs and Pharmaceutical Products
Reference Number: 22f1a0e13
Issuing Authority: Department of Military Affairs
Ministry: Ministry of Defence
Scope of Work and Objectives
This tender encompasses the procurement of essential drugs and pharmaceutical products. The key items include Amlodipine besylate 5 mg Tablets, Linezolid 600 mg Tablets, Clarithromycin 500 mg Tablets, and Inj Teriparatide 750 mcg. The primary objective of this tender is to ensure the availability of high-quality pharmaceuticals for use in military healthcare facilities.
Eligibility Criteria
To qualify for participation in this tender, bidders must be registered pharmaceutical manufacturers or authorized distributors. Bidders should provide evidence of their registration, along with compliance with relevant regulatory requirements pertinent to the procurement of pharmaceuticals. Proof of quality certifications must accompany the bid.
Technical Requirements
All products must adhere to the specified technical specifications, such as compliance with the Pharmaceuticals and Cosmetics Act, 1940, and applicable national and international quality standards. Each pharmaceutical product should be accompanied by detailed documentation including Certificate of Analysis (CoA) and compliance with Good Manufacturing Practices (GMP).
Financial Requirements
Bid submissions must include detailed financial quotations, reflecting clear pricing breakdowns for each item. Additionally, bidders are required to submit a Performance Security to ensure adherence to contract terms upon successful bid acceptance. It is crucial for bidders to realistically present their financial capability to support their deliverables without constraints.
Document Submission Details
Bidders are required to submit all relevant documents electronically via the designated portal. The submission must include the bid form, product specifications, quality certifications, and any additional supporting documentation that aligns with the tender requirements.
Special Provisions
Regarding Micro, Small, and Medium Enterprises (MSEs), provisions are made to encourage participation. MSEs must submit the necessary proofs to avail themselves of benefits under government programs.
Evaluation Process
The evaluation of bids will be conducted based on several parameters including price competitiveness, technical compliance, industry experience, and the ability to meet the outlined delivery timelines. The final selection will favor responsiveness and the ability to fulfill all contractual obligations effectively.
Delivery Locations
The successful bidders will be required to deliver the products to designated military healthcare facilities. Detailed delivery locations will be provided post-evaluation of bids.
Contact Information
For queries related to the tender, please refer to the official contact channels outlined in the tender document.
Additional Information
It is crucial for all participants to stay updated regarding any clarifications or amendments to the tender specifications. These updates will be communicated through the official portal.
Tender BOQ Items
9 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
- Additional Doc 1 (Requested in ATC)
- 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, demonstrating compliance with applicable Pharmaceuticals and Cosmetics regulations, and providing proof of quality certifications. Bidders must show their capability to deliver the specified drugs and pharmaceutical products, ensuring they are authorized to sell and distribute pharmaceuticals.
Bidders must submit various certificates, including Good Manufacturing Practice (GMP) certificates, Drug Manufacturing Licenses, and Certificates of Analysis (CoA) for each product. These certificates validate compliance with national and international quality standards necessary for medical supplies.
The registration process involves signing up on the official tender platform. Bidders are required to complete their profiles, after which they can submit documents in specified formats, ensuring all papers comply with guidelines set forth by the tendering authority. Accepted document formats are typically PDF and Word.
The EMD serves as a financial commitment from bidders, ensuring they adhere to the conditions set forth by the authority. Details on the amount and submission process for Performance Security requirements will be clearly outlined in the tender documentation.
Yes, there are distinct benefits for Micro, Small, and Medium Enterprises (MSEs), including relaxed qualification criteria and favorable conditions to encourage bidding participation. MSEs should submit the necessary documentation to substantiate their eligibility to avail of these provisions.
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