Tag: FDA Compliance

Validating Consistency in Cleanroom Pressure Differentials for Coated Tablet Production

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Validating Consistency in Cleanroom Pressure Differentials for Coated Tablet Production Validating Consistency in Cleanroom Pressure Differentials for Coated Tablet Production Introduction: In the pharmaceutical industry, maintaining a sterile environment is crucial for the production of high-quality coated tablets. Cleanrooms are designed to minimize contamination and ensure product safety. One essential aspect of cleanroom functionality is…

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Solid Dosage form, Tablets

Addressing Non-Compliance in Stability Testing for Coated Tablets

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Addressing Non-Compliance in Stability Testing for Coated Tablets Addressing Non-Compliance in Stability Testing for Coated Tablets Introduction: Stability testing is a critical component in the pharmaceutical industry, ensuring that drugs maintain their efficacy, safety, and quality over time. For coated tablets, this becomes even more crucial due to the additional complexity introduced by the coating…

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Solid Dosage form, Tablets

Controlling Humidity Variations in Compression Stages

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Controlling Humidity Variations in Compression Stages Controlling Humidity Variations in Compression Stages Introduction: In the realm of pharmaceutical manufacturing, maintaining the integrity and quality of solid dosage forms is paramount. Among the various stages of tablet production, the compression stage stands out as a critical phase where humidity control plays a decisive role. Humidity variations…

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Solid Dosage form, Tablets