GEM

Taluka Panchayat Vijayapur HPLC System Tender Karnataka 2025 NGSP IFCC CE FDA Compliant

Bid Publish Date

31-Dec-2025, 9:12 pm

Bid End Date

12-Jan-2026, 10:00 am

Value

₹5,00,000

Progress

Issue31-Dec-2025, 9:12 pm
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

1

Bid Type

Two Packet Bid

Categories 11

Tender Overview

Taluka Panchayat Vijayapur, operating under the Rural Development and Panchayat Raj Department of Karnataka, invites bids for a high-precision HPLC System designed for HbA1c and HbA2/HbF/HbA1c testing. Estimated value: ₹500,000. The system must offer multi-sample analysis capability, bi-directional LIS interface, and inbuilt system checks to ensure reagent and cartridge readiness. It should support dual programming for HbA1c and HbA2/HbF/HbA1c without reagent changes and report both NGSP and IFCC values on patient, control, and calibrator reports. Optional remote sample collection kit with 2-8°C stability for 14 days is preferred. System must be NGSP certified and traceable to IFCC; FDA and CE certifications are to be verified.

This tender emphasizes compliance with specific medical testing standards and interoperability with laboratory information systems, enabling seamless reporting and batch processing. Increased quantity flexibility up to 25% during contract execution is allowed, and detailed design drawings must be approved within 5 days of award. GST compliance is bidder’s responsibility and scope includes installation, testing, commissioning, and operator training.

Key differentiator: NGSP/IFCC traceability, dual HbA1c/HbA2 mode without reagent swaps, and LIS compatibility. Unique clause: option to adjust quantity within contract, with delivery timelines recalculated accordingly.

Technical Specifications & Requirements

  • Product: HPLC System for HbA1c/HbA2/HbF testing with dual-program capability
  • Samples handled concurrently: minimum required capacity to be specified by bidder; system must support high-throughput workflows
  • LIS interface: bi-directional lab interface capable of sending/receiving test data
  • Inbuilt checks: automated verification of cartridges, buffers, reagents, and waste before analysis
  • Reporting: dual NGSP and IFCC reporting on patient, control, and calibrator reports on a single output
  • Reagent switching: no reagent changes required when switching test modes
  • Capillary collection option: optional kit for remote sample collection with 2-8°C stability for 14 days
  • Certifications: NGSP certified and traceable to IFCC reference method; verify FDA and CE certification status
  • Delivery scope: supply, installation, testing, commissioning, operator training; statutory clearances if any
  • Documentation: detailed design drawings to be approved within 5 days post-award; approval or modification list provided within 5 days

Terms, Conditions & Eligibility

  • EMD: not specified in terms; bidder to confirm during submission
  • Delivery & flexibility: quantity may be increased/decreased by up to 25%; delivery period recalculated based on original period with minimum 30 days
  • Advance sample approval: 2 samples to be submitted within 5 days; buyer to approve or list modifications within 5 days; delay shifts delivery timeline without LD
  • GST: bidder bears GST; reimbursement as actual or applicable rates, subject to a cap
  • Scope of supply: includes supply, installation, testing, commissioning, operator training, and statutory clearances (if any)
  • GST & compliance: ensure GST registration, statutory compliance; no responsibility assumed for GST rates beyond quoted

Key Specifications

  • HPLC System with ≥1 analytical column path and minimum concurrent analyses: specify exact capacity

  • Bi-directional Laboratory Interface System (LIS) compatibility

  • Inbuilt pre-analysis system checks for cartridges, buffers, reagents, waste

  • Dual program mode: HbA1c and HbA2/Hb F/HbA1c without reagent change

  • Reagent-switching-free operation between HbA1c and HbA2/HbF/HbA1c

  • NGSP and IFCC reporting on a single patient report, control, and calibrator report

  • Capillary collection kit option with 2-8°C stability for 14 days

  • NGSP certified and traceable to IFCC reference method

  • FDA certification status verification

  • CE certification status verification

Terms & Conditions

  • Option to adjust bid quantity by up to 25% during order and contract currency

  • Advance sample approval: 2 samples within 5 days; potential delivery delay without LD

  • GST responsibility rests with bidder; reimbursement as actual or capped rate

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

Important Clauses

Payment Terms

GST handling by bidder; payment terms not specified in extract; confirm with bid documents

Delivery Schedule

Delivery period adjustable based on option clause; minimum 30 days; recalculated if quantity changes

Penalties/Liquidated Damages

Not specified in extract; confirm LD terms in final bid documents

Bidder Eligibility

  • Experience in supplying HPLC systems or equivalent medical laboratory equipment

  • Demonstrated LIS integration capability

  • NGSP certification and IFCC traceability or capable to achieve within warranty period

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Technical Specifications 1 Item

Item #1 Details

View Catalog
Category Specification Requirement
Set 1 Number of samples the Analyser is capable to analyse (minimum), concurrently: 10, 50, 100, 150 Or higher
Set 1 Availability of a bi-directional Laboratory Interface System (LIS): Yes, No
Set 1 HPLC system have an inbuilt system check facility which checks that all the system parameters (eg, cartridge, buffer, reagent, waste etc) are ready before the sample analysis: Yes, No
Set 1 HPLC system have a dual program mode to perform either HbA1c or HbA2/Hb F/HbA1c without changing any reagents or columns: Yes, No
Set 1 HPLC system should not require changing of reagents while switching from HbA1c to HbA2/Hb F/HbA1c testing mode: Yes, No
Set 1 HPLC System offers both NGSP & IFCC value reporting on the same patient report, control & calibrator report: Yes, No
Set 1 If the HPLC system have feature of capillary collection kit for remote sample collection with sample stability at 2-8 degree C for 14 days: Yes, No
Certifications HPLC System is NGSP (National Glycohemoglobin Standardisation Program) Certified and traceable to IFCC reference method: Yes, No
Certifications Whether the product  is US FDA certified: Yes, No
Certifications Whether the product  is CE European certified: Yes, No

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Required Documents

1

GST registration certificate

2

PAN card

3

Experience certificates for similar HPLC or medical laboratory equipment supply

4

Financial statements or turnover proof

5

EMD/Security deposit (if applicable) or explicit note of exemption

6

Technical bid documents demonstrating LIS compatibility and NGSP/IFCC compliance

7

OEM authorization or supplier authorization for the HPLC system

8

Manufacturer's technical specifications and warranty details

9

Installation, Testing & Commissioning plan

10

Training program outline for operators

Frequently Asked Questions

How to bid for the HPLC system tender in Karnataka?

Bidders must submit GST registration, PAN, experience certificates, financial statements, and EMD details (if applicable). Include OEM authorizations and detailed technical specifications demonstrating LIS compatibility and NGSP/IFCC traceability. Ensure 2 sample approvals within 5 days and confirm installation, testing, and commissioning plans.

What documents are required for HPLC system bidding in Vijayapur?

Required documents include GST certificate, PAN card, company turnover proof, prior experience certificates for similar HPLC systems, OEM authorization, and technical bid showing NGSP/IFCC compliance, along with installation and training plan and warranty terms.

What are the NGSP and IFCC reporting requirements for this HPLC?

The system must provide NGSP and IFCC reporting on patient, control, and calibrator reports from a single output. It must be NGSP certified and traceable to the IFCC reference method; verify FDA and CE status as applicable and include reporting without mode changes.

What is the delivery timeline and option clause for quantity changes?

Delivery period can be extended with an option clause allowing up to a 25% increase or decrease in quantity. Delivery time recalculates as (Increased/Original) × Original period with a minimum of 30 days; remaining terms remain aligned with award date.

What are the installation and training obligations for bidders?

Scope includes supply, installation, testing, commissioning, and operator training. The bidder must also provide any statutory clearances required. Detailed design drawings need buyer approval within 5 days of award; delays shift delivery without LD.

What about capillary collection kit and sample stability?

Capillary collection kit is an optional feature; if provided, it supports sample stability at 2-8°C for 14 days. Include this option in technical bid with exact kit specifications and compatibility with the HPLC system.

What certifications must the HPLC system have for this bid?

System must be NGSP certified and traceable to IFCC. Validate FDA and CE certifications if available; provide documentation of certification status and compatibility with dual HbA1c/HbA2/HbF testing modes.

Is there a required minimum concurrent sample analysis capacity?

The tender requires a capable HPLC system with multi-sample analysis capacity; specify exact concurrent sample capacity in the technical bid and ensure compatibility with LIS for data exchange.