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Tag: pharmaceutical formulation

Preventing Tablet Capping During High-Speed Compression

Posted on March 11, 2025 By Admin

Preventing Tablet Capping During High-Speed Compression Preventing Tablet Capping During High-Speed Compression Introduction: The pharmaceutical industry is ever-evolving, with technological advancements pushing the boundaries of speed and efficiency in drug manufacturing. Tablets, as a prevalent solid dosage form, are at the forefront of this evolution. However, with high-speed compression, challenges such as tablet capping can…

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Solid Dosage form, Tablets

Troubleshooting Residual Solvent Issues in Utility Lines for Sugar-Coated Tablets

Posted on March 10, 2025 By Admin

Troubleshooting Residual Solvent Issues in Utility Lines for Sugar-Coated Tablets Troubleshooting Residual Solvent Issues in Utility Lines for Sugar-Coated Tablets Introduction: In the pharmaceutical manufacturing landscape, sugar-coated tablets are a popular dosage form due to their aesthetic appeal and ease of swallowing. However, the manufacturing process involves various challenges, especially when it comes to managing…

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Solid Dosage form, Tablets

Addressing Heat Sensitivity of APIs During Validation of Coated Tablets

Posted on March 10, 2025 By Admin

Addressing Heat Sensitivity of APIs During Validation of Coated Tablets Addressing Heat Sensitivity of APIs During Validation of Coated Tablets Introduction: The pharmaceutical industry continuously strives to enhance the efficacy, stability, and safety of drug products. One of the critical aspects of drug formulation is the management of active pharmaceutical ingredients (APIs) that exhibit sensitivity…

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Solid Dosage form, Tablets

Managing Punch Adhesion Issues in Tablet Press Machines During Validation

Posted on March 10, 2025 By Admin

Managing Punch Adhesion Issues in Tablet Press Machines During Validation Managing Punch Adhesion Issues in Tablet Press Machines During Validation Introduction: In the pharmaceutical industry, the production of high-quality tablets is crucial for ensuring patient safety and therapeutic efficacy. One of the persistent challenges faced during tablet manufacturing is punch adhesion, commonly referred to as…

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Solid Dosage form, Tablets

Controlling Particle Fines During Powder Blending

Posted on March 10, 2025 By Admin

Controlling Particle Fines During Powder Blending Controlling Particle Fines During Powder Blending Introduction: In pharmaceutical manufacturing, especially in the production of solid dosage forms like tablets, the blending of powders is a critical step that determines the quality and efficacy of the final product. One of the persistent challenges in this process is the control…

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Solid Dosage form, Tablets

Real-Time Adjustment of Granulation Parameters for Uniformity

Posted on March 9, 2025 By Admin

Real-Time Adjustment of Granulation Parameters for Uniformity Real-Time Adjustment of Granulation Parameters for Uniformity Introduction: In the pharmaceutical industry, the uniformity of granulation is critical for ensuring the quality and efficacy of solid dosage forms, particularly tablets. Granulation is a pivotal step in the tablet manufacturing process, where powder particles are aggregated to form granules….

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Solid Dosage form, Tablets

Challenges in Binder Addition During Granulation

Posted on March 9, 2025 By Admin

Challenges in Binder Addition During Granulation Challenges in Binder Addition During Granulation Introduction: In the pharmaceutical industry, granulation is a crucial process in the production of solid dosage forms such as tablets. It involves the agglomeration of powder particles to form larger entities known as granules. One of the most critical components in the granulation…

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Solid Dosage form, Tablets

Investigating Poor API Distribution in Content Uniformity Tests

Posted on March 6, 2025 By Admin

Investigating Poor API Distribution in Content Uniformity Tests Investigating Poor API Distribution in Content Uniformity Tests Introduction: The pharmaceutical industry is heavily reliant on the precision and consistency of its products. One critical aspect of ensuring drug efficacy and safety is maintaining uniformity in the active pharmaceutical ingredient (API) distribution within solid dosage forms like…

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Solid Dosage form, Tablets

Ensuring Adequacy of Process Controls for Granulation Stages

Posted on March 5, 2025 By Admin

Ensuring Adequacy of Process Controls for Granulation Stages Ensuring Adequacy of Process Controls for Granulation Stages Introduction: Granulation is a critical process in the pharmaceutical industry, playing a pivotal role in the production of solid dosage forms such as tablets. It involves the aggregation of powder particles to form larger granules, which enhance the flow…

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Solid Dosage form, Tablets

Troubleshooting Heat Sensitivity Issues During Fluid Bed Drying

Posted on March 5, 2025 By Admin

Troubleshooting Heat Sensitivity Issues During Fluid Bed Drying Troubleshooting Heat Sensitivity Issues During Fluid Bed Drying Introduction: Fluid bed drying is a widely used method in pharmaceutical manufacturing for drying granules and powders before tablet compression. This process ensures uniform drying and improved product quality. However, the challenge of heat sensitivity in certain pharmaceutical compounds…

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Solid Dosage form, Tablets

Resolving Non-Uniform API Distribution in Extended Release Tablets Over Time

Posted on March 5, 2025 By Admin

Resolving Non-Uniform API Distribution in Extended Release Tablets Over Time Resolving Non-Uniform API Distribution in Extended Release Tablets Over Time Introduction: The pharmaceutical industry is constantly evolving, with a significant focus on developing efficient drug delivery systems. Extended release tablets are a crucial component of this landscape, designed to release active pharmaceutical ingredients (APIs) over…

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Solid Dosage form, Tablets

Difficulty in validating cleaning processes for high-viscosity formulations.

Posted on March 2, 2025 By Admin

Difficulty in validating cleaning processes for high-viscosity formulations. Difficulty in Validating Cleaning Processes for High-Viscosity Formulations Introduction: In the pharmaceutical industry, maintaining the integrity and quality of solid oral dosage forms, such as capsules, is of paramount importance. Among these, high-viscosity formulations present unique challenges in the cleaning process validation. This blog delves into the…

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Capsules (Hard & Soft Gelatin), Solid Oral Dosage Forms

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  • Aerosol Formulations
  • Capsules (Hard & Soft Gelatin)
  • Drug Discovery
  • External Preparations
  • GLP Guidelines
  • GMP Guidelines
  • Medical Devices
  • Parenteral Drug Manufacturing
  • Pharma Quality Control
  • Pharma Research
  • Schedule M
  • Solid Dosage form
  • Solid Oral Dosage Forms
  • Tablets
  • Tablets

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