Mapping Global Evidence to Indian Requirements: How to Repurpose US FDA & CE Data for CDSCO Submissions.
Global medical device manufacturers expanding into India often ask a common question: “Can we reuse our FDA or CE evidence for CDSCO registration?”The short answer: Yes, if the data is mapped, justified, and repurposed correctly. India’s regulatory framework under the CDSCO Medical Device Rules, 2017 (MDR 2017) strongly emphasises safety, performance, and clinical evaluation. This […]





