Drugs for DGLP - Department of Military Affairs - Indian Army
Baclofen 10mg tab,Glucosamine 500mg tab,Glyceryl trinitrate 2 point 6 mg tab NTG,Evening primerose
Tender Timeline
Tender Title: Drugs for DGLP
Reference Number: 4e3cd0b2
Issuing Authority: Department of Military Affairs, Ministry of Defence
Scope of Work and Objectives
The primary objective of this tender is to procure pharmaceuticals, including but not limited to Baclofen 10mg tablets, Glucosamine 500mg tablets, Glyceryl Trinitrate 2.6mg tablets (NTG), and Evening Primrose oil. The scope of work involves supplying a total quantity of 40,029 units of specified medications to ensure that the relevant healthcare facilities achieve their treatment goals efficiently. It is essential for bidders to fully understand the nature of the products and deliver them in a timely manner, adhering to quality standards.
Eligibility Criteria
To be considered eligible for this tender, bidders must meet several crucial criteria. This includes being a legally registered entity capable of supplying pharmaceuticals. Adequate experience in handling similar contracts and compliance with all legal requisites related to pharmaceutical procurement are mandatory. Bidders must demonstrate their ability to cater to the specific requirements of the Department of Military Affairs.
Technical Requirements
The products submitted must meet the technical specifications prescribed in the bid documentation. Each pharmaceutical product must comply with applicable quality standards and regulations enforced by the relevant health authorities. It is essential that all drugs are properly certified and meet the safety and efficacy criteria outlined by the Ministry of Defence.
Financial Requirements
Bidders should have sound financial standing and provide details of their financial capabilities. Pricing should reflect competitive market rates, and all costs must be detailed in the submitted bid. Financial documents must accompany the proposal to verify the economic viability of the bidder.
Document Submission Details
All bids must be submitted electronically. Bidders must ensure that their proposals are complete and submitted within the required time frame. Detailed instructions regarding the submission process, including any platform or format specifications, will be provided in the tender documents. Efforts must be made to ensure that all documents are presented clearly and concisely, meeting the required standards.
Special Provisions
Recognizing the importance of fostering growth within the sector, special provisions may be afforded to Micro, Small, and Medium Enterprises (MSEs) and startups as part of this tender process. Eligible businesses will be notified of their entitlements and potential benefits during the bidding process.
Evaluation Process
The evaluation process will be conducted methodically to assess submissions against predefined criteria. Bids will be evaluated based on technical capabilities, pricing, and adherence to submission guidelines. Potential bidders are advised to provide thorough and transparent documentation to facilitate this process.
Delivery Locations
Successful bidders will be required to deliver the pharmaceuticals to specified locations as detailed in the tender documents. Timely delivery is critical, and bidders should outline their proposed delivery timelines within their submissions.
Contact Information
For queries regarding the bid or additional information, bidders are encouraged to consult the official contact point designated in the tender documents. It is crucial to ensure clear and open communication for successful bid submissions.
Tender BOQ Items
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Financial Information
Evaluation and Technical Information
Tender Documents
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Frequently Asked Questions
The eligibility requirements include being a registered entity capable of supplying pharmaceuticals. Bidders must possess adequate experience in similar contracts and demonstrate compliance with legal requisites related to pharmaceutical procurement. A sound financial standing is also required alongside the ability to meet the specified technical and quality standards.
Bidders must provide valid certificates that showcase compliance with local regulations and pharmaceutical safety standards. This may include manufacturing licenses, GMP (Good Manufacturing Practices) certifications, and any other relevant regulatory approvals. Proper documentation will play a crucial role in the evaluation process.
The registration process involves creating a profile on the designated procurement platform, where bidders can fill out necessary details and upload required documents. Following the initial registration, participants must carefully follow additional guidelines to ensure their bids meet all requirements specified in the tender documents.
Bids must be submitted electronically via the designated procurement platform. Accepted document formats typically include PDF, DOCX, and XLSX. Bidders should ensure that all documents are organized, complete, and conform to the tender guidelines to avoid disqualification.
The tender process acknowledges the significance of Micro, Small, and Medium Enterprises (MSEs) by potentially providing benefits such as reserved quotas, easier qualification criteria, and simplified documentation processes. MSEs are encouraged to participate as this tender seeks to foster inclusive growth within the pharmaceutical supply sector.
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