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GEM

Government Tender Published for PHG0296,R0533,13778100,174925,SLHVR33RS,15240-062,D3861,Q10210,Q33221

Bid Publish Date

23-Oct-2024, 4:42 pm

Bid End Date

13-Nov-2024, 5:00 pm

Progress

Issue23-Oct-2024, 4:42 pm
AwardPending
Explore all 3 tabs to view complete tender details

Quantity

13

Categories 10

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!

Documents 4

GeM-Bidding-7060043.pdf

Main Document

BOQ Document

BOQ

BOQ Document

BOQ

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

Bill of Quantities (BOQ) 9 Items

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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Frequently Asked Questions

## FAQs
What are the eligibility requirements for participating in this tender?

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.

What certificates are required for submission?

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.

How can bidders register to participate in the tender?

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.

What document formats are accepted for submissions?

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.

What are the technical specifications for the consumables?

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.

What quality standards must the products meet?

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.

What compliance requirements must bidders fulfill?

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.

Are there specific testing criteria for items?

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.

What is the Earnest Money Deposit (EMD) requirement?

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.

What are the performance security requirements post-award?

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.

What are the payment terms for the contract?

Payment terms will be defined in the contract, typically including conditions for milestone payments or payment upon completion of delivery and acceptance of goods.

What considerations are there for price evaluation?

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.

How can submissions be made?

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.

What are the key timelines and deadlines for this tender?

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.

How will the evaluation and selection process work?

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.

How will results be communicated to the bidders?

Results will be communicated through official notifications on the GeM platform, where selected vendors will be informed about the outcomes of the bidding process.

What benefits are provided for MSEs in this tender?

MSEs are encouraged to participate, receiving special implications in the tendering process aimed at increasing suppliers’ equity and fostering competitive growth within the industry.

What provisions are available for startups?

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.

Are local content policies applicable?

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.