Bid Publish Date
23-Oct-2024, 4:42 pm
Bid End Date
13-Nov-2024, 5:00 pm
Progress
Quantity
13
Indian Council Of Medical Research (icmr) announces a tender for PHG0296, R0533, 13778100, 174925, SLHVR33RS, 15240-062, D3861, Q10210, Q33221. Quantity: 13. Submission Deadline: 13-11-2024 17: 00: 00. Last date to apply is approaching fast!
Main Document
BOQ
BOQ
GEM_GENERAL_TERMS_AND_CONDITIONS
| Item # | Title | Description | Quantity | Unit | Consignee | Delivery (Days) |
|---|---|---|---|---|---|---|
| 1 | PHG0296 | Human recombinant PLGF protein (25ug) | 1 | kit | [email protected] | 60 |
| 2 | R0533 | TurboFect Transfection reagent | 1 | kit | [email protected] | 60 |
| 3 | 13778100 | Lipofectamine RNAi Max (0.1ml) | 1 | kit | [email protected] | 60 |
| 4 | 174925 | 96U Nunclon Sphera 300Ul each (pack of 8) | 3 | kit | [email protected] | 60 |
| 5 | SLHVR33RS | Millex PVDF Syringe filter pore size 0.45uM | 2 | kit | [email protected] | 60 |
| 6 | 15240-062 | Antibiotic-Antimycotic 100X | 2 | kit | [email protected] | 60 |
| 7 | D3861 | BODIPY 581/591 C11 (Lipid peroxidation sensor) 1mg | 1 | kit | [email protected] | 60 |
| 8 | Q10210 | Qubit RNA BR Assay Kit (100 assays) | 1 | kit | [email protected] | 60 |
| 9 | Q33221 | Qubit RNA integrity and quality Assay kit (75 Assays) | 1 | kit | [email protected] | 60 |
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The eligibility requirements include being a registered entity with the ability to supply the specified chemical consumables, complying with regulatory standards, and meeting financial stability criteria as assessed through relevant documentation.
Participants are required to possess valid business registration certificates, quality assurance certificates for the chemicals, and any other regulatory compliance documents that confirm adherence to standards relevant to medical research consumables.
Bidders must complete the registration process via the Government e-Marketplace (GeM) platform, ensuring that all required documentation is uploaded in compliance with the submission guidelines provided in the tender.
Submitted documents must be in PDF format to ensure compatibility and facilitate the evaluation process. Bidders should verify that all necessary documentation is included in this format.
Technical specifications will vary by item but generally include performance metrics, quality certifications, and adherence to standards set forth by the ICMR for laboratory-grade consumables and reagents necessary for medical research.
Products must meet the requisite quality standards set forth by the ICMR, including any ISO certifications or specific research-grade standards pertinent to medical consumables.
Bidders must ensure compliance with all relevant regulations and standards applicable to chemical procurement and use in medical research, as well as adherence to environmental health and safety regulations.
Yes, there may be specific testing criteria outlined in the tender documents that detail the required performance and quality benchmarks that products must meet before acceptance.
The Earnest Money Deposit (EMD) requirement will be specified in the tender documents. Bidders are advised to carefully review the tender to determine the exact deposit amount needed for participation.
Successful bidders must provide a performance security, details of which will be specified in the tender documents. This security ensures compliance with the terms of the contract and successful execution of orders.
Payment terms will be defined in the contract, typically including conditions for milestone payments or payment upon completion of delivery and acceptance of goods.
The price evaluation will consider not only the quoted prices but also the quality, compliance with specifications, and overall value offered by the bidder, ensuring the best option for the ICMR.
Submissions must be made through the Government e-Marketplace (GeM), where electronic bids can be uploaded according to the specified guidelines in the tender documents.
Bidders must adhere to the timelines outlined in the tender documents, including submission dates, opening dates for bids, and validity periods for offers, to ensure participation.
Bids will be evaluated based on predefined criteria that consider technical compliance, financial offers, and overall value, with successful bidders recommended for award based on their total scores.
Results will be communicated through official notifications on the GeM platform, where selected vendors will be informed about the outcomes of the bidding process.
MSEs are encouraged to participate, receiving special implications in the tendering process aimed at increasing suppliers’ equity and fostering competitive growth within the industry.
Startups are provided with unique opportunities within this tender framework, allowing them to showcase innovative products and solutions as part of a broader initiative to enhance medical research.
Compliance with local content and procurement rules may be mandated, fostering national capabilities and ensuring broader access to local suppliers within the framework of government procurement initiatives.
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Main Document
BOQ
BOQ
GEM_GENERAL_TERMS_AND_CONDITIONS