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Medical Products Regulation in India

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Public Notice:

Sr. No.TitleFile No.DatePDF Link
1Manufacturing and marketing of unapproved FDC’sFile No. 4-01/2023-DC (Misc. 3)11 April 2025PDF Download

Gazette Notification:

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Recent Posts

  • Revised Schedule M, Drugs Rules, 1945
  • Provision for auto-generated Market Standing Certificate and Non-Conviction Certificate for licenced medical device.
  • “New Drugs” in India
  • Submission of online application for extension of time to comply with revised Sch M on ONDLS portal – www.statedrugs.gov.in
  • National Regulatory Authority (NRA): CDSCO

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