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Pharma cos with over Rs 250 cr turnover have to adopt good manufacturing practices within 6 months: Mandaviya

by AIP Online Bureau | Aug 3, 2023 | Health, Indian News, Non-Life, Regulation, Risk Management

Recently, drug regulators inspected 162 units and 14 public testing labs and major issues found during inspections are poor documentation, lack of process and analytical validations, absence of quality failure investigation, absence of internal product quality review...

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