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CDSCO Clarifies AI Medical Device Regulations Under MDR 2017
CDSCO has issued guidance on regulating AI-enabled medical devices under the Medical Devices Rules (MDR), 2017. This clarification aims to streamline the approval process for software-based medical products, ensuring safety and efficacy. The updated regulations are crucial for developers and healthcare providers navigating the evolving landscape of medical technology.
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"Regulatory clarity is always a win for innovation in healthcare!"
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