As part of the plan, in addition to the revised schedule M good manufacturing practices (GMP) compliance, the apex drug regulator will focus on risk-based inspection, increased monitoring and sampling, and extensive sensitization and enforcement.
The plan also involves directing all states and Union territories to share spurious and substandard drugs data with the Centre.
Esta historia es de la edición January 03, 2025 de Mint Kolkata.
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Esta historia es de la edición January 03, 2025 de Mint Kolkata.
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