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Fee Schedule

This page provides links to the current CDSCO and SUGAM portal fee schedules for licensing, inspection, and other regulatory services related to medical devices.

Official sources: CDSCO; SUGAM portal; Bureau of Indian Standards; IMDRF

Fee Schedule Overview

Fee Schedule Overview

Purpose: CDSCO charges fees for regulatory services including license applications, renewals, and inspections. Fees are prescribed in Schedule 1 of the Medical Devices Rules 2017.

Types of fees:

  • Manufacturing license application fees (varies by device class)
  • Import license fees
  • License renewal fees
  • GMP inspection fees
  • Testing/sample analysis fees (at notified labs)

How fees are determined:

  • Device class (A, B, C, D)
  • License type (new vs. renewal)
  • Number of manufacturing sites or product lines
  • Inspection scope and complexity

Fee payment:

  • Fees submitted through SUGAM portal during application
  • Payment made via e-payment gateway
  • Fee receipt required for application processing

Current fee amounts: For current fee schedule, consult:

  • Medical Devices Rules 2017, Schedule 1
  • CDSCO official website (Medical Devices Fees section)
  • SUGAM portal (updated annually)

Official resources: CDSCO; SUGAM portal; Bureau of Indian Standards; IMDRF