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CDSCO has issued the Guidance Document on Medical Device Software to align India’s regulatory requirements with globally harmonized practices and streamline approvals.
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Health Ministry removes cough syrups from Schedule K, restricts their sale in smaller villages to licensed pharmacies.
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The newly appointed Drug Inspectors are authorized to exercise the powers and perform the duties as specified in Sections 21 and 22 of the Drugs and Cosmetics Act and the Medical Devices Rules.
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