Tag: USP Guidelines

Resolving Over-Lubrication Issues in Immediate Release Tablets

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Resolving Over-Lubrication Issues in Immediate Release Tablets Resolving Over-Lubrication Issues in Immediate Release Tablets Introduction: Immediate release tablets are a mainstay in the pharmaceutical industry, offering quick onset of action and ease of administration. However, the formulation and manufacturing of these tablets present unique challenges, particularly with lubrication. Over-lubrication can compromise tablet quality, affecting disintegration…

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Solid Dosage form, Tablets

Evaluating Impact of Packaging Materials on Tablet Stability Profiles

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Evaluating Impact of Packaging Materials on Tablet Stability Profiles Evaluating Impact of Packaging Materials on Tablet Stability Profiles Introduction: In the pharmaceutical industry, the stability of tablets is paramount to ensure efficacy and safety throughout their shelf life. Packaging materials play a crucial role in protecting tablets from environmental factors such as moisture, light, oxygen,…

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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