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  Class A & B Devices have been regulated since April 1 and manufacturers who were registered but not Licensed on April 1 were allowed to continue manufacturing and selling while the state and central government regulators sought compliance and audit certification etc . Similar written

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Shows noble and ambitious intent of PM Narendra Modi: Rajiv Nath   Association of Indian Medical Industry (AiMeD) Forum Coordinator Rajiv Nath has hailed Promotion of Research and Innovation in Pharma MedTech Sector (PRIP) Scheme as a “noble and ambitious intent” of Prime Minister Narendra Modi,

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Medical devices sector can’t be regulated alongside drugs: Rajiv Nath   The Association of Indian Medical Device Industry (AiMeD), an umbrella organization representing the interest of over 1200 manufacturers of medical devices, has reiterated its demand for a separate regulatory mechanism for medical device industry.

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New Medical Device Bill, 2023 will prove catastrophic for domestic players: Rajiv Nath    The New Drugs, Medical Devices and Cosmetics Bill, 2023 is fraught with loopholes and repercussions for domestic medical device industry and must be recalled for further deliberations and corrections failing which Prime

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MedTech Policy Conclave 2023, organized after the introduction of the National Medical Devices Policy, gets a robust response from all stakeholders who underpinned the major pain points and the way forward   MedTech Policy Mahotsava Conclave 2023, organized by Medgate Today, witnessed a remarkable turnout

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MedTech Policy Conclave 2023, organized after the introduction of the National Medical Devices Policy, gets a robust response from all stakeholders who underpinned the major pain points and the way forward   MedTech Policy Mahotsava Conclave 2023, organized by Medgate Today, witnessed a remarkable

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