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GEM

Bids are Invited For High Performance Liquid Chromatography (HPLC) System in FARIDABAD, HARYANA

Bid Publish Date

13-Nov-2025, 3:11 pm

Bid End Date

11-Dec-2025, 1:00 pm

EMD

₹80,000

Latest Corrigendum Available

Progress

Issue13-Nov-2025, 3:11 pm
Corrigendum04-Dec-2025
AwardPending
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Quantity

1

Bid Type

Two Packet Bid

Categories 11

Public procurement opportunity for Translational Health Science And Technology Institute (thsti) High Performance Liquid Chromatography (HPLC) System (Q3) in FARIDABAD, HARYANA. Quantity: 1 issued by. Submission Deadline: 11-12-2025 13: 00: 00. View full details and respond.

Documents 5

GeM-Bidding-8583025.pdf

Main Document

Other Documents

OTHER

CATALOG-Specification-1

CATALOG Specification

Buyer uploaded ATC document

ATC

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

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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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Historical Data

Required Documents

1

Experience Criteria

2

Past Performance

3

Certificate (Requested in ATC)

4

OEM Authorization Certificate

5

Additional Doc 1 (Requested in ATC)

6

Additional Doc 2 (Requested in ATC)

7

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

8

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

Corrigendum Updates

1 Update
#1

Update

04-Dec-2025

Extended Deadline

11-Dec-2025, 1:00 pm

Opening Date

11-Dec-2025, 1:30 pm