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Indian Air Force Paracetamol 10mg/ml Infusion Tender 100 ml bottle, ISI/MDR Compliant, CDSCO 2017, 2026

Bid Publish Date

20-Jun-2026, 10:04 am

Bid End Date

30-Jun-2026, 11:00 am

Progress

Issue20-Jun-2026, 10:04 am
AwardPending
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Quantity

6000

Bid Type

Two Packet Bid

Key Highlights

  • Regulatory alignment with MDR 2017 and DCGI/CDSCO approvals for paracetamol infusion
  • GS1 barcodes required across primary, secondary, and tertiary packaging levels
  • Batch-wise NABL test reports and DCGI/CDSCO compliance demonstrated for each shipment
  • Cold chain maintenance mandated; strict recalls and replacement/refund obligations
  • Shelf life rule: two years or more with five-sixth shelf life remaining at supply date
  • Mandatory drug licence details: Manufacturing/Sales/Distribution numbers and CDSCO licensing
  • Undertakings for stock replacement if expiry approaches or safety concerns arise
  • No BOQ items specified; procurement revolves around regulatory-compliant infusion products

Categories 3

Tender Overview

  • Organization: Indian Air Force (Department Of Military Affairs) seeking Paracetamol 10mg/ml Infusion in 100 ml bottle. Location not specified; procurement scope targets pharmaceutical infusion stock for medical use. Estimated value and EMD are not disclosed in the data. Key differentiator: strict regulatory compliance with CDSCO, MDR 2017, and GS1 barcode encoding across packaging levels. Unique requirement includes replacement obligation for recalled products and 6-month expiry risk management. This tender emphasizes cold chain maintenance and batch-test availability per DCGI and CDSCO norms.

Technical Specifications & Requirements

  • Product: Paracetamol 10mg/ml Infusion in 100 ml bottle.
  • Standards/Regulatory: MDR 2017, DCGI/CDSCO approvals, GS1 barcodes on primary/secondary/tertiary packaging, and Drug Licence details (Mfg/Sales/Distribution).
  • Documentation: Need batch-level NABL test reports and compliance with Schedule P of Drugs and Cosmetics Rules; ensure Not-Standard-Quality recall protocol.
  • Packaging/Labeling: Must follow DGCI/CDSCO labelling and packaging norms; barcoding to encode mandated information.
  • Shelf Life: Minimum two years or more as per DCGI/CDSCO; delivery with five-sixth shelf life remaining on supply date.
  • Cold Chain: Maintaining cold chain as per regulatory guidance; availability of test reports for each batch.
  • Quality/Recall: Immediate notification and replacement/refund on quality concerns; recall procedures to be executed at supplier cost.
  • Delivery/Test: Availability of batch-wise testing and quality assurance documentation; compliance with drug control norms.

Terms, Conditions & Eligibility

  • EMD: Not specified in the data; bidders should anticipate standard government EMD requirements.
  • Documentation: Mandatory drug licence numbers, manufacturing/sales/distribution certificates, CDSCO license validity, and MDR compliance documentation.
  • Recall/Refund: Supplier to replace or refund unconsumed stock if safety issues arise; obligation to withdraw questionable lots.
  • Warranty/Support: Not explicitly defined; subject to CDSCO/MDR compliance and batch testing acceptance.
  • Compliance: Must meet barcoding, labelling, packaging, and cold-chain standards; batch-wise NABL test reports required.
  • Penalties: Not specified; implied through standard regulatory non-compliance and recall costs.

Key Specifications

  • Product category: Paracetamol 10mg/ml Infusion in 100 ml bottle

  • Regulatory: MDR 2017 compliant, DCGI/CDSCO approvals

  • Packaging: GS1 barcodes at primary, secondary, tertiary levels

  • Shelf life: minimum 24 months with five-sixth shelf life remaining on supply

  • Quality: NABL test report available for each batch; standard testing per regulatory norms

  • Recall: supplier must replace or refund unconsumed stock in case of safety concerns

  • Cold chain: maintained per Drug Controller General of India requirements

Terms & Conditions

  • EMD—not disclosed in data; bidders should anticipate standard EMD submission

  • Delivery contingent on regulatory approvals and cold chain readiness

  • Warranty and post-supply support governed by CDSCO/MDR compliance and recall terms

Important Clauses

Payment Terms

Not specified; bidders should expect standard government payment terms post-inspection and batch acceptance

Delivery Schedule

Delivery timelines linked to regulatory clearance and cold-chain readiness; no explicit dates in data

Penalties/Liquidated Damages

Not specified; penalties may be implied through regulatory non-compliance and recall costs

Bidder Eligibility

  • Demonstrated experience supplying regulated pharmaceutical injections

  • Valid drug licences (Manufacturing/Sales/Distribution) and CDSCO MDR compliance

  • Ability to provide batch-wise NABL test reports and GS1 barcode packaging

Additional Tender Data

Commercial Details

Tender Category

Goods

Bid To RA

No

Bid To RA Enabled

Yes

Item Category

Paracetamol 10mg/ml Infusion In100 Ml Bottle

Authority Records

MINISTRY OF DEFENCEMILITARY AFFAIRS DEPARTMENT

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Documents 4

GeM-Bidding-9446727.pdf

Main Document

Other Documents

OTHER

Buyer uploaded ATC document

ATC

GEM General Terms and Conditions Document

GEM_GENERAL_TERMS_AND_CONDITIONS

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Required Documents

1

GST registration certificate

2

PAN card

3

Drug Licence numbers (Manufacturing/Sales/Distribution) and issue/validity dates

4

CDSCO/MDR compliance certificates

5

OEM authorization (if applicable)

6

NABL batch test reports for each supplied batch

7

DCGI/CDSCO approvals and product registration details

8

Quality and compliance certificates, including packaging and labeling standards

9

Any recall history documentation or supplier performance records

Frequently Asked Questions

How to bid for the paracetamol infusion tender in India with regulatory compliance

Bidders must submit drug licences (Manufacturing/Sales/Distribution), CDSCO/MDR compliance, and batch NABL test reports. Ensure GS1 barcode packaging, cold chain readiness, and provide recall handling plans. The procurement requires compliance with DCGI/CDSCO norms and packaging labeling as per Drug Rules.

What documents are required for the IAF paracetamol infusion bid 2026

Provide GST registration, PAN, drug licences, CDSCO MDR certificates, OEM authorizations if applicable, NABL batch test reports, and regulatory approvals. Include product registration details and recall policies; ensure data align with Drugs and Cosmetics Rules Schedule P.

What are the technical specs for Paracetamol 10mg/ml infusion in 100 ml

Product must be Paracetamol 10mg/ml infusion in 100 ml bottle with two-year shelf life, GS1 barcoding, and MDR 2017 adherence. Also require NABL batch test documentation and DCGI/CDSCO licensing validity for each batch shipped.

What are the EMD and payment terms for this IAF procurement

EMD amount is not disclosed in the tender data; bidders should expect standard government EMD procedures. Payment terms typically follow post-delivery acceptance and regulatory compliance, but exact percentages or timelines are not specified in the provided information.

How is shelf life managed for paracetamol infusion shipments

Shelf life must be a minimum of two years with at least five-sixth of shelf life remaining at the time of supply. If stock approaches expiry, replacement or refund obligations apply, per the recall clause and regulatory norms.

What regulatory standards must be met for these medicines

Manufacturing and supply must comply with MDR 2017, DCGI/CDSCO approvals, and Schedule P of Drugs and Cosmetics Rules. Packaging must feature GS1 barcodes at all packaging levels, with NABL batch testing reported for each batch.

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