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…
Class A, B, C, D
CDSCO registration / import license
- ▸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…
Class A, B, C, D
SFDA device listing / market authorization
- ▸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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