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Tag: Pharmaceutical manufacturing

Troubleshooting Failures in Compressed Air Quality Tests for Compression Machines

Posted on June 2, 2025 By Admin

Troubleshooting Failures in Compressed Air Quality Tests for Compression Machines Troubleshooting Failures in Compressed Air Quality Tests for Compression Machines Introduction: In the pharmaceutical industry, the quality of compressed air used in tablet compression machines is paramount. Compressed air serves as a critical utility, influencing both product quality and operational efficiency. Ensuring that this air…

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Solid Dosage form, Tablets

Troubleshooting Non-Adherence of Coating Layers in Multi-Layer Tablets

Posted on June 2, 2025 By Admin

Troubleshooting Non-Adherence of Coating Layers in Multi-Layer Tablets Troubleshooting Non-Adherence of Coating Layers in Multi-Layer Tablets Introduction: In the pharmaceutical industry, multi-layer tablets are gaining prominence due to their ability to deliver multiple drugs or achieve controlled release profiles. However, these complex formulations often face challenges, particularly with the adherence of coating layers. Ensuring that…

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Solid Dosage form, Tablets

Ensuring Adequacy of Water Flow Rates in Purified Water Systems

Posted on June 2, 2025 By Admin

Ensuring Adequacy of Water Flow Rates in Purified Water Systems Ensuring Adequacy of Water Flow Rates in Purified Water Systems Introduction: In the pharmaceutical industry, purified water is a critical component used in various manufacturing processes, including the production of solid dosage forms such as tablets. Ensuring the adequacy of water flow rates in purified…

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Solid Dosage form, Tablets

Troubleshooting Failures in Cleaning Validation for Coating Equipment

Posted on June 1, 2025 By Admin

Troubleshooting Failures in Cleaning Validation for Coating Equipment Troubleshooting Failures in Cleaning Validation for Coating Equipment Introduction: In the pharmaceutical industry, the cleaning validation of coating equipment is a critical process that ensures the safety and efficacy of drug products. Cleaning validation verifies that residues from the manufacturing process, including active pharmaceutical ingredients (APIs), excipients,…

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Solid Dosage form, Tablets

Validating Spray Gun Settings for Even Coating Distribution

Posted on June 1, 2025 By Admin

Validating Spray Gun Settings for Even Coating Distribution Validating Spray Gun Settings for Even Coating Distribution Introduction: In the pharmaceutical industry, ensuring that tablets have an even coating is crucial not only for aesthetic purposes but also for the functionality of the dosage form. The coating protects the active pharmaceutical ingredient (API), controls release profiles,…

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Solid Dosage form, Tablets

Validating Water Purification Systems for Tablet Manufacturing Processes

Posted on May 30, 2025 By Admin

Validating Water Purification Systems for Tablet Manufacturing Processes Validating Water Purification Systems for Tablet Manufacturing Processes Introduction: In the pharmaceutical industry, water is not just an ingredient; it is a critical component in the manufacturing of tablets. The purity and quality of water used in tablet manufacturing are paramount, as they directly affect the safety…

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Solid Dosage form, Tablets

Ensuring Accuracy in Compression Force Sensors During Tablet Press Validation

Posted on May 29, 2025 By Admin

Ensuring Accuracy in Compression Force Sensors During Tablet Press Validation Ensuring Accuracy in Compression Force Sensors During Tablet Press Validation Introduction: In the pharmaceutical industry, precision in tablet manufacturing is paramount. Ensuring the accuracy of compression force sensors during tablet press validation is critical for maintaining the quality and uniformity of tablets. These sensors play…

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Solid Dosage form, Tablets

Troubleshooting Failures in Rinse Sampling for Fluid Bed Dryers During Validation

Posted on May 28, 2025 By Admin

Troubleshooting Failures in Rinse Sampling for Fluid Bed Dryers During Validation Troubleshooting Failures in Rinse Sampling for Fluid Bed Dryers During Validation Introduction: Rinse sampling is a critical step in the validation of fluid bed dryers within pharmaceutical manufacturing. Ensuring that no residues of active pharmaceutical ingredients (APIs) or cleaning agents remain is essential for…

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Solid Dosage form, Tablets

Validating Cleaning Protocols for High-Speed Compression Lines

Posted on May 28, 2025 By Admin

Validating Cleaning Protocols for High-Speed Compression Lines Validating Cleaning Protocols for High-Speed Compression Lines Introduction: In the pharmaceutical industry, ensuring the cleanliness of equipment used in tablet production is crucial for maintaining product quality and safety. High-speed compression lines are integral to the efficient production of tablets, but they also pose significant challenges when it…

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Solid Dosage form, Tablets

Troubleshooting Label Placement Accuracy on Tablet Bottles

Posted on May 28, 2025 By Admin

Troubleshooting Label Placement Accuracy on Tablet Bottles Troubleshooting Label Placement Accuracy on Tablet Bottles Introduction: In the pharmaceutical industry, the accurate placement of labels on tablet bottles is crucial for ensuring product compliance, safety, and traceability. Labels provide essential information such as dosage instructions, expiration dates, and batch numbers. Any inaccuracies in label placement can…

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Solid Dosage form, Tablets

Validating Airborne Particle Monitoring Systems in Cleanrooms

Posted on May 27, 2025 By Admin

Validating Airborne Particle Monitoring Systems in Cleanrooms Validating Airborne Particle Monitoring Systems in Cleanrooms Introduction: In pharmaceutical manufacturing, the integrity of cleanrooms is paramount to ensuring product safety and efficacy. Airborne particle monitoring systems are critical components of cleanroom environments, as they ensure that the levels of particulate matter remain within acceptable limits. These systems…

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Solid Dosage form, Tablets

Ensuring Robustness in Layer Adhesion for Bilayer Tablet Equipment Validation

Posted on May 27, 2025 By Admin

Ensuring Robustness in Layer Adhesion for Bilayer Tablet Equipment Validation Ensuring Robustness in Layer Adhesion for Bilayer Tablet Equipment Validation Introduction: In the realm of pharmaceutical manufacturing, bilayer tablets have emerged as a significant advancement, offering multiple benefits such as the ability to combine incompatible substances, controlled release profiles, and patient convenience. However, the manufacturing…

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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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