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.
Bu hikaye Mint Bangalore dergisinin January 03, 2025 sayısından alınmıştır.
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Bu hikaye Mint Bangalore dergisinin January 03, 2025 sayısından alınmıştır.
Start your 7-day Magzter GOLD free trial to access thousands of curated premium stories, and 9,000+ magazines and newspapers.
Already a subscriber? Giriş Yap
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