GEM

Invitation to Bid - U10701 Y Multipurpose labeling tape 0.75 inches x 500 inches yellow,1620177 Immun-Blot PVDF Membran

Bid Publish Date

21-Nov-2024, 4:12 pm

Bid End Date

12-Dec-2024, 5:00 pm

Bid Opening Date

12-Dec-2024, 5:30 pm

Value

₹2,91,400

Progress

Issue21-Nov-2024, 4:12 pm
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

26

Category

U10701 Y Multipurpose labeling tape 0.75 inches x 500 inches yellow

Bid Type

Two Packet Bid

Categories 18

Indian Council Of Medical Research (icmr) invites bids for U10701 Y Multipurpose labeling tape 0. 75 inches x 500 inches yellow, 1620177 Immun-Blot PVDF Membrane, D2438-5X10ML Dimethyl sulfoxide DMSO, BR100012 Cytiva Sensor chip CM5 pack of 3, T-200-C Pipette tips 200ul clear tips, TF-300 Pipette tips 10ul filter tips clear. Quantity: 26. Submission Deadline: 12-12-2024 17: 00: 00. Submit your proposal before the deadline.

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Bill of Quantities (BOQ) 6 Items

Item # Title Description Quantity Unit Consignee Delivery (Days)
1 U10701 Y Multipurpose labeling tape 0.75 inches x 500 inches yellow U10701 Y Multipurpose labeling tape 0.75 inches x 500 inches yellow 2 rolls konari 60
2 1620177 Immun-Blot PVDF Membrane 1620177 Immun-Blot PVDF Membrane 1 pack konari 60
3 D2438-5X10ML Dimethyl sulfoxide DMSO D2438-5X10ML Dimethyl sulfoxide DMSO 1 pack konari 60
4 BR100012 Cytiva Sensor chip CM5 pack of 3 BR100012 Cytiva Sensor chip CM5 pack of 4 2 pack konari 60
5 T-200-C Pipette tips 200ul clear tips T-200-C Pipette tips 200ul clear tips 10 packs konari 60
6 TF-300 Pipette tips 10ul filter tips clear TF-300 Pipette tips 10ul filter tips clear 10 packs konari 60

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Required Documents

1

Experience Criteria

2

Past Performance

3

Certificate (Requested in ATC)

4

OEM Authorization Certificate

5

Compliance of BoQ specification and supporting document *In case any bidder is seeking exemption from Experience / Turnover Criteria

6

the supporting documents to prove his eligibility for exemption must be uploaded for evaluation by the buyer

Frequently Asked Questions

What are the eligibility requirements for tender participation?

The eligibility requirements for participation in the tender include being a registered entity capable of supplying the necessary medical consumables. Bidders must provide experience criteria and records of past performance to demonstrate their capability. Additionally, OEM Authorization Certificates and compliance with BoQ specifications must be submitted. MSEs may avail exemptions regarding previous experience by providing necessary supporting documentation.

What types of certificates are required for the bid?

Bidders are required to submit several certificates with their bid, including experience criteria documentation, past performance records, OEM Authorization Certificates (if applicable), and compliance certifications as per BoQ specifications. This ensures that all submitted products meet the necessary quality and industry standards.

How can I register for this tender?

To register for this tender, interested bidders must follow the registration process specified in the official procurement portal. They should create a vendor profile, submit the required documents, and ensure that they comply with all listed eligibility criteria. Accessing and reviewing the detailed guidelines provided in the tender documents is essential for a successful registration.

What document formats are accepted for submission?

All submissions must be made in the prescribed document formats indicated within the tender documentation. This typically includes PDF or other specified formats compatible with electronic submission systems. Bidders are urged to refer to the official requirements to ensure compliance.

What are the specific technical specifications for the consumables?

The technical specifications including those for the multipurpose labeling tape, PVDF Membrane, DMSO, Sensor chips, and pipette tips, are detailed within the BoQ document associated with the tender. It is imperative for bidders to ensure that the products offered meet these specifications to qualify for consideration.

What quality standards must be adhered to during the project?

All supplied products must meet the quality standards established by the Department of Health Research, as prescribed in the tender documentation. This includes compliance with industry standards for medical consumables to ensure reliability and consistency in the workflow of research activities.

Are there testing criteria for the supplied items?

Yes, there are stringent testing criteria that must be met by all provided items. Suppliers are expected to demonstrate compliance with these testing benchmarks as outlined in the tender documents, ensuring that the goods meet necessary safety and efficacy requirements.

What are the details regarding the Earnest Money Deposit (EMD)?

The Earnest Money Deposit (EMD) details are specified in the tender documentation. Bidders are required to submit EMD along with their bid proposal as a security to indicate the seriousness of their participation in the bidding process. Failure to provide the required EMD may result in bid disqualification.

What performance security is required upon selection?

Bidders selected for this tender will be required to submit a performance security which is a financial guarantee ensuring adherence to contractual obligations. The details regarding the amount and format of performance security will be provided in the tender documents.

What are the payment terms outlined in the tender?

The payment terms established will specify the conditions under which the payment will be made once goods are delivered and accepted. Bidders should consult the tender documents for explicit details regarding payment schedules and conditions of payment upon delivery.

How will price evaluations be conducted?

Price evaluations will take into account the total costs presented by bidders in their proposals, while also factoring in compliance with technical specifications and overall value offered. The evaluation committee will assess bids comprehensively to identify the most advantageous option.

What submission methods are applicable for this tender?

Submissions for this tender must be conducted through the specified electronic procurement platform outlined in the tender. Bidders should ensure they use the correct channels and adhere to submission guidelines to guarantee that their proposals are accepted.

When will result notifications be sent to bidders?

Notifications regarding the results of the evaluation and selection process will be communicated to all bidders once the evaluation is complete. Specific timelines for these notifications will be detailed in the final tender documents.

What benefits can MSEs gain from this tender?

Micro, Small, and Medium Enterprises (MSEs) can benefit from various provisions outlined in the government procurement policies. This includes exemptions regarding experience criteria, aimed at encouraging MSE participation and promoting their growth within the sector.

Are there provisions for startups participating in the tender?

Startups are encouraged to participate in the tender, provided they meet the specifications and quality standards outlined. They may also benefit from provisions that support their participation under government procurement policies.

How does this tender align with 'Make in India' initiatives?

This tender supports the 'Make in India' initiative by prioritizing local manufacturing and procurement standards. Suppliers participating in this tender are encouraged to comply with local content rules and demonstrate their capability to contribute to the development of domestic manufacturing in the healthcare sector.