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Tag: pharmaceutical best practices

Validating Adequacy of Clean Steam Systems for Film-Coating Equipment

Posted on March 2, 2025 By Admin

Validating Adequacy of Clean Steam Systems for Film-Coating Equipment Validating Adequacy of Clean Steam Systems for Film-Coating Equipment Introduction: In the pharmaceutical industry, ensuring the adequacy of clean steam systems is crucial for the successful operation of film-coating equipment used in tablet production. Clean steam, often used for sterilization and process control, must be free…

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Solid Dosage form, Tablets

Troubleshooting Non-Adherence to Cleanroom Validation Standards for Particle Monitoring

Posted on March 2, 2025 By Admin

Troubleshooting Non-Adherence to Cleanroom Validation Standards for Particle Monitoring Troubleshooting Non-Adherence to Cleanroom Validation Standards for Particle Monitoring Introduction: In the pharmaceutical industry, maintaining a pristine environment is paramount to ensuring product quality and patient safety. Cleanrooms play a crucial role in this process, particularly in the manufacturing of solid dosage forms like tablets. A…

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Solid Dosage form, Tablets

Poor reproducibility in monitoring capsule sealing strength.

Posted on March 2, 2025 By Admin

Poor reproducibility in monitoring capsule sealing strength. Poor reproducibility in monitoring capsule sealing strength. Introduction: In the pharmaceutical industry, the integrity of capsule sealing is crucial to ensure product efficacy, patient safety, and compliance with regulatory standards. Capsules, both hard and soft gelatin, are a preferred dosage form due to their ease of administration and…

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

Validating Clean Steam Systems for Extended Release Tablet Equipment

Posted on March 1, 2025 By Admin

Validating Clean Steam Systems for Extended Release Tablet Equipment Validating Clean Steam Systems for Extended Release Tablet Equipment Introduction: In the pharmaceutical industry, ensuring the sterility and safety of products is paramount, especially in the manufacturing of extended-release tablets. Clean steam systems play a crucial role in maintaining the integrity of the manufacturing process, as…

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Solid Dosage form, Tablets

Validating Spray Guns in Coating Machines for Consistency

Posted on March 1, 2025 By Admin

Validating Spray Guns in Coating Machines for Consistency Validating Spray Guns in Coating Machines for Consistency Introduction: In the pharmaceutical industry, coating tablets is a critical process that ensures product stability, controls the release of the active ingredient, and enhances the product’s aesthetic appeal. The role of spray guns in coating machines is vital as…

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Solid Dosage form, Tablets

Controlling Humidity Variations in Compression Stages

Posted on March 1, 2025 By Admin

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

Posts pagination

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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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