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Tag: Equipment Calibration

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

Addressing Non-Uniform Temperature Mapping in Fluid Bed Dryers During Validation

Posted on March 1, 2025 By Admin

Addressing Non-Uniform Temperature Mapping in Fluid Bed Dryers During Validation Addressing Non-Uniform Temperature Mapping in Fluid Bed Dryers During Validation Introduction: Fluid bed dryers are critical components in the pharmaceutical manufacturing process, particularly in the production of solid dosage forms such as tablets. The uniformity of temperature within these dryers is crucial to ensure product…

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Solid Dosage form, Tablets

Developing Equipment Qualification Protocols for Tablet Compression Machines

Posted on March 1, 2025 By Admin

Developing Equipment Qualification Protocols for Tablet Compression Machines Developing Equipment Qualification Protocols for Tablet Compression Machines Introduction: In the pharmaceutical industry, the production of tablets is a critical process that demands precision and adherence to stringent quality standards. Equipment qualification for tablet compression machines is a vital step to ensure that the machinery used in…

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Solid Dosage form, Tablets

Ensuring Robustness in Steam Quality Testing for Enteric-Coated Tablet Equipment

Posted on March 1, 2025 By Admin

Ensuring Robustness in Steam Quality Testing for Enteric-Coated Tablet Equipment Ensuring Robustness in Steam Quality Testing for Enteric-Coated Tablet Equipment Introduction: In the pharmaceutical industry, enteric-coated tablets are crucial due to their ability to withstand the acidic environment of the stomach and deliver active ingredients to the intestine. The production of these tablets requires precise…

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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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