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Regulatory authorities play a crucial role in monitoring and setting standards for Rabeprazole impurities to ensure the safety and efficacy of the drug.
Yes, Rabeprazole impurities are evaluated during clinical trials to assess their safety and ensure compliance with regulatory standards.
Yes, impurities in Rabeprazole can impact the drug's stability.
Rabeprazole impurities are stored at a regulated room temperature of 2-8°C or as specified on the Certificate of Analysis (CoA).
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