GEM

National Animal Resource Facility For Biomedical Research Recombinase Amplification Kit Lyoready Enzymes and Hybri Detect Strips Tender India 2025

Bid Publish Date

05-Dec-2025, 5:36 pm

Bid End Date

26-Dec-2025, 6:00 pm

Progress

Issue05-Dec-2025, 5:36 pm
AwardPending
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Quantity

15

Category

Recombinase Amplification Kit Lyoready Enzymes and Reagents

Bid Type

Two Packet Bid

Categories 4

Tender Overview

National Animal Resource Facility For Biomedical Research invites bids for the procurement of Recombinase Amplification Kit Lyoready Enzymes and Hybri Detect strips along with associated reagents (Plasmid Midi kit 25 reactions, dialysis membrane, nuclease-free water) for use in biomedical research. The scope includes supply, installation, testing, commissioning, operator training, and any required statutory clearances. The tender emphasizes compliance with Make in India authorisation, MSME/NSIC exemptions where applicable, and OEM turnover criteria. A key clause allows a potential 50% quantity increase/decrease at bid or contract stage. Unique requirements include end-user certificate handling and a three-year turnover evaluation for bidders and OEMs.

Technical Specifications & Requirements

  • No explicit product specifications are published; bidders should reference the listed items: Recombinase Amplification Kit Lyoready enzymes, Hybri detect strips, Plasmid Midi kit (25 reactions), dialysis membrane with dimensions (flat width 24.26mm, diameter 14.3mm, capacity 1.61mL per cm length 1m), and nuclease-free water (6X 1.5mL).
  • Scope of supply encompasses delivery, installation, testing, commissioning, operator training, and any statutory clearances.
  • Required documentation implies adherence to Make in India authorization and OEM turnover criteria; compliance with safety and quality standards is implied by the need for audited financials to verify turnover.

Terms, Conditions & Eligibility

  • EMD: Not specified in data; bidders must provide applicable security as per buyer terms.
  • Experience: Supply experience with government/PSU or reputable private organizations; end-user certificate provision in Buyer’s standard format if requested.
  • Turnover: Minimum average annual turnover over the last three years to be demonstrated; OEM turnover criteria apply to the offered product category.
  • Delivery: Scope includes installation, testing, commissioning; delivery period linked to order and potential quantity variations up to 50%.
  • Documentation: Must include GST, PAN, experience certificates, audited financials or CA certificates; Make in India authorization; OEM authorizations; technical bid documents.

Key Specifications

  • Recombinase Amplification Kit Lyoready enzymes and related reagents

  • Hybri detect strips for diagnostic use

  • Plasmid Midi kit 25 reactions

  • Dialysis membrane: flat width 24.26 mm, diameter 14.3 mm, capacity 1.61 mL per cm, length 1 m

  • Nuclease-free water, 6X 1.5 mL tubes

  • Scope includes supply, installation, testing, commissioning, and operator training

  • Compliance with Make in India authorization and OEM turnover criteria

Terms & Conditions

  • EMD amount not disclosed; bidders must provide security as per buyer terms

  • Quantity variations up to 50% possible at contract award and during currency

  • Turnover verification required for bidder and OEM from last three financial years

Important Clauses

Payment Terms

Payment terms and schedule are not specified; bidders should expect standard government terms and potential advance/partial payments per contract

Delivery Schedule

Delivery period linked to order; extended delivery time may apply with quantity adjustments as per option clause

Penalties/Liquidated Damages

Penalties or LD clauses are not detailed; bidders should anticipate standard contract LD for late delivery or non-compliance

Bidder Eligibility

  • Experience in supplying to Govt/PSU or reputed private organizations

  • Demonstrated turnover meeting OEM/product category requirements (last 3 years)

  • Make in India authorization and OEM authorization for offered products

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Bill of Quantities (BOQ) 5 Items

Item # Title Description Quantity Unit Consignee Delivery (Days)
1 Recombinase Amplification Kit Lyoready Enzymes and Reagents Recombinase Amplification Kit Lyoready Enzymes and Reagents 5 kit [email protected] 60
2 Millenia Genline Hybri detect strips Millenia Genline Hybri detect strips 2 kit [email protected] 60
3 Plasmid Midi kit 25 reactions Room Temperature storage Plasmid Midi kit 25 reactions Room Temperature storage 1 kit [email protected] 60
4 Dialysis membrane 50, Av. Flat width 24.26mm, Av. Diameter 14.3mm, capacity 1.61mL per cm Length 1m Dialysis membrane 50, Av. Flat width 24.26mm, Av. Diameter 14.3mm, capacity 1.61mL per cm Length 1m 5 box [email protected] 60
5 Nuclease free water 6X 1.5mL Nuclease free water 6X 1.5mL 2 box [email protected] 60

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Required Documents

1

GST registration certificate

2

PAN card

3

Experience certificates for supply to Govt/PSU/renowned private organizations

4

Audited Balance Sheets or CA certificates indicating turnover (last 3 years)

5

OEM authorization for the offered products

6

Make in India authorization certificate

7

End User Certificate in Buyer's standard format (if requested)

8

Technical bid documents demonstrating compliance with listed items

9

Any NSIC/MSME exemption certificates (if applicable)

Frequently Asked Questions

How to bid for Recombinase Amplification Kit tender India 2025?

Bidders must submit GST, PAN, experience certificates, audited turnover, OEM authorization, Make in India certificate, and technical bid documents. Ensure evidence of past govt/PSU supply, and demonstrate compliance with turnover criteria for the OEM and bidder. Include End User Certificate if requested and confirm supply scope covers installation, testing, commissioning, and operator training.

What documents are required for this India diagnostic kit tender?

Submit GST certificate, PAN card, three-year turnover proofs (audited balance sheets or CA certificate), experience certificates for govt/PSU supply, OEM authorizations, Make in India authorization, and technical bid detailing listed items. End User Certificate may be requested in the buyer format.

What are the specified items in the BOQ for this procurement?

The BOQ lists five items: Recombinase Amplification Kit Lyoready enzymes, Hybri detect strips, Plasmid Midi kit (25 reactions), dialysis membrane (24.26 mm width, 14.3 mm diameter, 1.61 mL per cm, 1 m length), and nuclease-free water (6X 1.5 mL). No separate quantity data provided.

What turnover criteria apply to bidders and OEMs for this bid?

The bidder and OEM must show a minimum average annual turnover over the last three financial years ending 31 March prior year. If company less than 3 years old, use completed years post-incorporation. Documentation must be certified by CA/Cost Accountant or audited balance sheets.

Is there an option to adjust quantity under this tender?

Yes. The purchaser reserves the right to increase or decrease quantity up to 50% of bid quantity at contract placement and during currency, with delivery time adjustments calculated as (Additional quantity / Original quantity) × Original delivery period.

What certifications are required for Make in India eligibility in this tender?

Bidders must provide Make in India authorization certificate. OEMs should demonstrate Make in India certification for the offered products and ensure compliance with related government procurement norms.

What delivery and training obligations are expected in this procurement?

Scope includes supply, installation, testing, commissioning, and operator training; the contract may require statutory clearances where applicable and training of operators to ensure proper use of Recombinase Amplification Kit and Hybri detect strips.

When can bidders expect end-user certificate requirements to apply?

End User Certificate requirements may be requested if bidders insist on it; when invoked, provide in the buyer’s standard format along with the supply documentation and ensure compliance with the buyer’s format.