§ COMPARE REGULATORS

CDSCO vs SFDA: Medical Device Regulatory Comparison

Compare the medical device registration pathways, classification, and regulatory requirements of CDSCO (India) vs SFDA (Saudi Arabia).

CDSCO

Central Drugs Standard Control Organization (India)

India

India's CDSCO regulates medical devices under the Medical Devices Rules 2017 (amended 2020). India uses a four-class system (A, B, C, D). India is the fastest-growing major medical device market globa

CLASSES

Class A, B, C, D

PATHWAY

CDSCO registration / import license

KEY FUNCTIONS
  • Medical device registration
  • Import license (Form MD-14)
  • Clinical investigation approval
  • Quality management system audit
  • Adverse event reporting

SFDA

Saudi Food and Drug Authority

Saudi Arabia

The SFDA regulates medical devices in Saudi Arabia under the Medical Devices Interim Regulation. Saudi Arabia is increasingly aligning with international standards (IMDRF) and has introduced mandatory

CLASSES

Class A, B, C, D

PATHWAY

SFDA device listing / market authorization

KEY FUNCTIONS
  • Device listing (MDMA)
  • Conformity assessment
  • Adverse event reporting
  • GCC harmonization
  • Import control

MedFlux monitors both CDSCO and SFDA in real time — every regulatory change, safety alert, and market signal delivered in under 90 seconds.

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