Consumables for Medical Research
76743 miCURY Exosome cell Urine CSF kit,1106 DNA blood mini kit 250 rxn,19155 Protease 7.5 AU lyoph
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Tender Title: Consumables for Medical Research
Tender Reference Number: 11d5e934f
Issuing Authority/Department: Department of Health Research, Ministry of Health and Family Welfare
The Consumables for Medical Research tender aims to procure essential medical research items that are crucial for advancing health research initiatives. This tender encompasses a broad scope of consumables, specifically designed for laboratory research applications, including but not limited to miCURY Exosome cell Urine CSF kits, DNA blood mini kits, Protease reagents, and preservation tubes.
Scope of Work and Objectives:
The objective is to supply a total of 14 items spanning various categories essential for medical research. The successful supplier will be expected to ensure high-quality standards, timely delivery, and compliance with all regulatory requirements. The list of consumables includes:
- miCURY Exosome Cell Urine CSF Kits
- DNA Blood Mini Kits (250 reactions)
- Protease (7.5 AU lyophilized)
- UltraPure DEPC-Treated Water
- TriZOL LS Reagents (100ml)
- CF-DNA cf RNA Preservation Tubes (10ml)
This procurement process aims to support research related to diagnostics, drug discovery, and genetic studies, ultimately contributing to enhanced healthcare solutions.
Eligibility Criteria:
Eligible bidders must meet certain pre-qualifications, including:
- Registration as a legal entity in relevant sectors.
- Proven experience in supplying similar items for medical research.
- Valid certifications and compliance with health sector regulations.
Technical Requirements:
Vendors must adhere to stringent technical specifications outlined in the tender. This includes quality assurance measures, capacity for scalability in production, and the ability to meet specific delivery schedules.
Financial Requirements:
Bidders are required to submit a detailed financial proposal that outlines the pricing for each item listed. Competitive pricing will be an essential criterion during the evaluation process alongside compliance with the Earnest Money Deposit (EMD) requirements, which ensures the bidder's commitment to the tender process.
Document Submission Details:
Proposals, along with required documents (like financial bids, company registration details, and quality certifications), must be submitted through the designated procurement portal by the specified deadline. Vendors should ensure all documents are submitted in the accepted formats to avoid disqualification.
Special Provisions:
The tender is designed with provisions to encourage participation from Micro, Small, and Medium Enterprises (MSEs) and Startups, promoting an inclusive approach to supplier diversity. It also adheres to 'Make in India' policies, encouraging local production and procurement.
Evaluation Process:
Bids will be evaluated based on a multi-factor approach considering:
- Compliance with eligibility criteria.
- Technical specifications matching.
- Financial proposals in relation to market standards.
- Commitment to delivery timelines.
Delivery Locations:
Items will be delivered to designated research facilities and laboratories as specified in the final contract agreement.
Contact Information:
For any inquiries or further clarification regarding this tender, interested parties may refer to the contact details available on the procurement portal.
Tender BOQ Items
8 ItemsGeneral Information
Financial Information
Evaluation and Technical Information
Tender Documents
4 DocumentsDocuments Required from Seller
- Experience Criteria
- Past Performance
- OEM Authorization Certificate
- 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 for this tender include being a registered entity in the respective field, possessing prior experience in supplying medical research consumables, and holding valid certifications. Bidders will be assessed based on their compliance with health sector regulations, ensuring they can deliver quality research materials consistently.
Participants must possess relevant certificates that confirm their compliance with industry standards for medical supplies. This includes quality management system certifications (like ISO) and any specific licenses required by governmental health authorities, along with proof of prior supply experience.
To participate in the tender, interested suppliers must go through a registration process on the designated procurement platform. This involves filling out and submitting necessary forms along with proof of eligibility, which may include company registration documents, financial statements, and relevant certifications.
All documentation must be submitted in specified formats such as PDF or DOC, as stipulated in the tender guidelines. Suppliers should ensure that all files are legibly scanned and are free from corruption to facilitate a smooth evaluation process.
The evaluation process involves a detailed review of submitted bids focusing on the technical specifications and financial proposals. Each bid is assessed against established criteria for compliance, quality, and cost-effectiveness, leading to the selection of the most suitable supplier based on the best value and adherence to project timelines.
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