§ COMPARE REGULATORS

CDSCO vs INVIMA: Medical Device Regulatory Comparison

Compare the medical device registration pathways, classification, and regulatory requirements of CDSCO (India) vs INVIMA (Colombia).

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

INVIMA

INVIMA — Colombia Medical Device Regulatory Authority

Colombia

INVIMA is the national regulatory authority responsible for medical device oversight in Colombia. It manages device registration, market surveillance, and adverse event reporting within the Latin Amer

CLASSES

Class I, IIa, IIb, III

PATHWAY

INVIMA registration

KEY FUNCTIONS
  • Device registration
  • Market surveillance
  • Adverse event reporting
  • Import/export control

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

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§ OTHER COMPARISONS