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The firm acknowledged that releasing OOS compounded preparations reflects a deviation from internal quality assurance procedures and obligation to notify patients and prescribers. But the FDA found that no corrective actions were provided to address the failure to notify patients and prescribers when OOS results were identified

Comparing different encapsulation technologies confirmed the general pattern: encapsulation improves bioavailability , plain powder does not

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doi: 10.1002/mc.23741 125 ChenBFuWJieCZhangGLiZLiuYet al