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Tag: Equipment Maintenance

Troubleshooting Failures in Temperature Mapping for Fluid Bed Dryers

Posted on June 5, 2025 By Admin

Troubleshooting Failures in Temperature Mapping for Fluid Bed Dryers Troubleshooting Failures in Temperature Mapping for Fluid Bed Dryers Introduction: In the pharmaceutical industry, the drying process is a critical step in the production of solid dosage forms such as tablets. Fluid bed dryers play a significant role in ensuring that the drying process is efficient…

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Solid Dosage form, Tablets

Validating Clean Steam Systems for Sustained Release Tablet Coating Machines

Posted on June 3, 2025 By Admin

Validating Clean Steam Systems for Sustained Release Tablet Coating Machines Validating Clean Steam Systems for Sustained Release Tablet Coating Machines Introduction: In the pharmaceutical industry, the precision and reliability of equipment are crucial to ensuring product efficacy and safety. Among these, sustained release tablet coating machines play a pivotal role in controlling the release profile…

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Solid Dosage form, Tablets

Managing Residue Build-Up in Spray Guns for Coating Equipment Cleaning Validation

Posted on May 31, 2025 By Admin

Managing Residue Build-Up in Spray Guns for Coating Equipment Cleaning Validation Managing Residue Build-Up in Spray Guns for Coating Equipment Cleaning Validation Introduction: In the pharmaceutical industry, maintaining the integrity of coating equipment is vital for ensuring product quality and regulatory compliance. Spray guns, integral to the coating process, often face challenges related to residue…

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Solid Dosage form, Tablets

Managing Calibration Failures in Dissolution Testing Equipment for Coated Tablets

Posted on May 31, 2025 By Admin

Managing Calibration Failures in Dissolution Testing Equipment for Coated Tablets Managing Calibration Failures in Dissolution Testing Equipment for Coated Tablets Introduction: Dissolution testing is a critical quality control measure in the pharmaceutical industry, especially for coated tablets. It ensures that the drug releases its active ingredients at the intended rate and extent. However, calibration failures…

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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 Effectiveness for Blending Equipment Used for Multi-API Tablets

Posted on May 24, 2025 By Admin

Validating Cleaning Effectiveness for Blending Equipment Used for Multi-API Tablets Validating Cleaning Effectiveness for Blending Equipment Used for Multi-API Tablets Introduction: In the pharmaceutical industry, ensuring the cleanliness of manufacturing equipment is paramount, particularly when it comes to producing multi-API (Active Pharmaceutical Ingredient) tablets. These tablets, which contain more than one active ingredient, require meticulous…

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Solid Dosage form, Tablets

Troubleshooting Failures in Equipment Calibration for Weight Variation Control

Posted on May 22, 2025 By Admin

Troubleshooting Failures in Equipment Calibration for Weight Variation Control Troubleshooting Failures in Equipment Calibration for Weight Variation Control Introduction: In the pharmaceutical manufacturing industry, the production of tablets requires meticulous attention to detail to ensure consistent quality and efficacy. One critical aspect of tablet production is maintaining precise weight variation control, which directly impacts dosage…

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Solid Dosage form, Tablets

Troubleshooting Failures in Compression Force Validation for High-Speed Presses

Posted on May 22, 2025 By Admin

Troubleshooting Failures in Compression Force Validation for High-Speed Presses Troubleshooting Failures in Compression Force Validation for High-Speed Presses Introduction: In the fast-paced world of pharmaceutical manufacturing, high-speed tablet presses are indispensable assets that enable large-scale production of solid dosage forms. These machines are designed to efficiently compress powders into tablets, making them crucial in meeting…

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Solid Dosage form, Tablets

Addressing Cross-Contamination Risks in Blending Equipment During Cleaning Validation

Posted on May 19, 2025 By Admin

Addressing Cross-Contamination Risks in Blending Equipment During Cleaning Validation Addressing Cross-Contamination Risks in Blending Equipment During Cleaning Validation Introduction: The pharmaceutical industry is committed to ensuring the safety and efficacy of its products. One critical component of this commitment is the prevention of cross-contamination, particularly in the manufacturing of solid dosage forms like tablets. Blending…

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Solid Dosage form, Tablets

Addressing Failures in Cleaning Validation for High-Speed Compression Machines

Posted on May 16, 2025 By Admin

Addressing Failures in Cleaning Validation for High-Speed Compression Machines Addressing Failures in Cleaning Validation for High-Speed Compression Machines Introduction: In the pharmaceutical industry, maintaining stringent cleanliness standards for manufacturing equipment is crucial to ensure product safety and efficacy. High-speed compression machines, integral to tablet production, are no exception. Cleaning validation is a critical process that…

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Solid Dosage form, Tablets

Troubleshooting Calibration Failures in Dissolution Testing Equipment

Posted on May 10, 2025 By Admin

Troubleshooting Calibration Failures in Dissolution Testing Equipment Troubleshooting Calibration Failures in Dissolution Testing Equipment Introduction: Dissolution testing is a critical process in the pharmaceutical industry, serving as a quality control measure to ensure the efficacy and safety of tablets and other solid dosage forms. Calibration of dissolution testing equipment is essential for accurate and reliable…

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Solid Dosage form, Tablets

Troubleshooting Failures in Layer Adhesion During Bilayer Tablet Equipment Validation

Posted on May 6, 2025 By Admin

Troubleshooting Failures in Layer Adhesion During Bilayer Tablet Equipment Validation Troubleshooting Failures in Layer Adhesion During Bilayer Tablet Equipment Validation Introduction: Bilayer tablets have emerged as a significant advancement in pharmaceutical dosage forms, offering the potential for controlled release, improved patient compliance, and enhanced therapeutic efficacy. However, their manufacturing presents unique challenges, particularly concerning layer…

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Solid Dosage form, Tablets

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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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