Determine whether a local clinical investigation is required for your CDSCO submission — and if so, assess India's feasibility as a clinical study location for your device indication.
Based on your indication, these types of centres typically have the infrastructure and patient volume for interventional device studies.
This screener provides indicative guidance. A formal India clinical study feasibility assessment includes site identification, investigator qualification review, patient recruitment modelling, and ethics committee timelines. Our team has conducted feasibility assessments for Class C/D devices across interventional cardiology, neurovascular, and peripheral vascular indications.
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