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Chittaranjan Locomotive Works Sterile Hypodermic Syringes Procurement Bardhaman West Bengal IS 10258 Part 1 2026

Bid Publish Date

03-Jun-2026, 7:39 pm

Bid End Date

15-Jun-2026, 4:00 pm

Progress

Issue03-Jun-2026, 7:39 pm
AwardPending
Explore all 4 tabs to view complete tender details

Quantity

240

Bid Type

Two Packet Bid

Tender Overview

Chittaranjan Locomotive Works (Indian Railways) invites bids for Single Use Sterile Hypodermic Syringes for Human Use conforming to IS 10258 (Part 1). The procurement location is BARDHAMAN, WEST BENGAL – 713101. Key product requirements include syringes with an included needle, a shielding cap or shield, and a specified nominal capacity (ml) with packaging details such as number of pieces per pack. Suppliers must ensure drug and cosmetic act compliance and possess a valid Medical Device license issued by the competent authority under MDR 2017. The tender references the ability to adjust quantities by up to 25% during contract execution and requires advance sample approval prior to bulk manufacturing. The absence of a BOQ indicates a focus on standard product compliance rather than quantity-led pricing. Unique inspection arrangements include post-receipt inspection at the consignee site and pre-dispatch inspection at seller premises only if selected. This tender emphasizes regulatory compliance, sample-based validation, and adherence to statutory licensing.

Technical Specifications & Requirements

  • Product category: Single-use sterile hypodermic syringes for human use
  • Needle: Included, with needle cap/shield for safety
  • Syringe features: Defined by number of pieces per syringe set; nominal capacity to be specified
  • Packaging: Pack composition details (pieces per pack) to be provided
  • Shelf life: Residual shelf life requirement to be stated
  • Certifications: Drugs and Cosmetic Act 1940, Medical Device Rules (MDR 2017 as amended); valid Medical Device license required
  • Regulatory: Compliance with IS 10258 (Part 1), along with applicable drug regulation approvals
  • Quality/Testing: Buyer may test conformity to contract specifications and approve advance samples before bulk supply
  • Inspection: Post-receipt inspection at the consignee site; pre-dispatch inspection at seller premises only if clause elected

Terms, Conditions & Eligibility

  • Option clause: Purchaser may increase/decrease quantity up to 25% of bid/contract quantity; extended delivery time calculated if option exercised
  • GST: Bidder to determine GST; reimbursement as per actuals or applicable rate (whichever is lower)
  • Inspection: Post-receipt inspection by designated authority (Sr. DMO/KGH/CLW/CRJ)
  • Sample clause: Advance sample approval required within 10 days of award; 5-day response for modification list; bulk supply aligned to approved sample
  • Delivery & penalties: Delivery timelines anchored to last delivery order date; LD provisions to be followed if approvals are delayed
  • Documentation: Submission must include required compliance and licensing documentation as per supplier terms

Key Specifications

    • Product: Single Use Sterile Hypodermic Syringes for Human Use
    • Key standard: IS 10258 (Part 1)
    • Certifications: Drugs and Cosmetic Act 1940; Medical Device Rules MDR 2017; valid Medical Device license
    • Packaging: Pack size details (pieces per pack) to be specified
    • Safety: Needle included with cap/shield for protection
    • Regulatory: Compliance with MDR 2017 amendments and licensing

Terms & Conditions

  • Mandatory IS 10258 (Part 1) compliance with MDR 2017 licensing

  • Up to 25% quantity variation allowed during contract execution

  • Post-receipt inspection at consignee site; pre-dispatch inspection if applicable

  • Advance sample approval required within 10 days of award

  • GST handling as per actuals or lower applicable rate; bidder bears GST exposure

Important Clauses

Payment Terms

GST payable by bidder; reimbursement at actuals or applicable rate; no implied GST from buyer

Delivery Schedule

Delivery starts after order date; option to extend time proportional to quantity variation with minimum 30 days

Penalties/Liquidated Damages

LD applicable if delivery or sample approvals are delayed beyond contracted windows; terms to be finalized per contract

Bidder Eligibility

  • Must hold valid Medical Device license for syringes under MDR 2017

  • Must demonstrate IS 10258 (Part 1) compliance or equivalence

  • Experience in supplying sterile medical devices to government or large-scale procurement

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

No

Item Category

Single Use Sterile Hypodermic Syringes for Human Use Conforming to IS 10258 (Part 1) (Q2)

Authority Records

MINISTRY OF RAILWAYS
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Documents 5

GeM-Bidding-9417819.pdf

Main Document

CATALOG-Specification-1

CATALOG Specification

Other Documents

OTHER

Other Documents

OTHER

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
PRODUCT INFORMATION Needle included Yes
PRODUCT INFORMATION Syringe type based on number of pieces Three Piece Syringe (Barrel and Piston, plunger and plunger stopper are two separate components of different materials)
PRODUCT INFORMATION Needle cap or shield to protect the needle Yes
PRODUCT INFORMATION Nominal Capacity of Syringe (ml) >2 - 5
PACKAGING Number of pieces in a Pack 100
SHELF LIFE Residual shelf life of the product Agree to provide residual shelf life of atleast 75% of total shelf life at the time of delivery to the consignee
CERTIFICATIONS Compliance to Drugs and Cosmetic Act 1940 and Medical Device Rules (MDR) 2017 as amended till date Yes
CERTIFICATIONS Availability of valid Medical Device license for the product issued from the competent authority Yes

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Required Documents

1

GST registration certificate

2

PAN card

3

Medical Device license (valid) issued by competent authority

4

Experience certificates demonstrating capability to supply sterile syringes

5

Technical compliance certificates and IS 10258 (Part 1) alignment

6

OEM authorization (if applicable)

7

Financial statements or turnover proof as required by tender terms

8

Any other documents specifically requested under buyer terms

Frequently Asked Questions

Key insights about WEST BENGAL tender market

How to bid for CLW sterile syringes procurement in Bardhaman?

Bidders must hold a valid Medical Device license, ensure IS 10258 (Part 1) compliance, and submit GST, PAN, and technical documents. Advance sample submission is due within 10 days of award, with a 5-day response window for modifications and adherence to 25% quantity variation terms.

What documents are required for CLW syringe tender in West Bengal?

Required documents include GST registration, PAN, Medical Device license, supplier experience certificates, IS 10258 alignment certificates, OEM authorizations if applicable, and financial statements demonstrating turnover. Include technical bid and any certificates requested under buyer terms.

What standards must syringes meet for this CLW procurement?

Syringes must conform to IS 10258 (Part 1) and comply with Drugs and Cosmetic Act 1940; MDR 2017 amendments must be adhered to, with a valid Medical Device license from a competent authority.

What is the delivery variation allowed in this Tender?

The purchaser may increase/decrease quantity up to 25% of bid/contract quantity, and extended delivery time is calculated as (additional quantity/original quantity) × original delivery period, with a minimum of 30 days.

What is required for advance sample approval in this tender?

Within 10 days of award, submit 2 advance samples for buyer approval; the buyer responds within 5 days with modifications; bulk supply must align to the approved sample, else re-sampling or contract termination may occur.

Are there post-delivery inspections for the CLW syringe contract?

Yes, post-receipt inspection will be conducted at the consignee site by Sr. DMO/KGH/CLW/CRJ; pre-dispatch inspection at seller premises is applicable only if the ATC specifies it.

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