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Tag: Pharmaceutical Industry

Troubleshooting Failures in Compressed Air Distribution for Coated Tablets

Posted on March 4, 2025 By Admin

Troubleshooting Failures in Compressed Air Distribution for Coated Tablets Troubleshooting Failures in Compressed Air Distribution for Coated Tablets Introduction: In the pharmaceutical industry, the production of coated tablets is a sophisticated process that requires precision and adherence to strict quality standards. Compressed air plays a vital role in various stages of tablet manufacturing, including coating,…

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Solid Dosage form, Tablets

Addressing Cross-Contamination Risks in Shared Utility Lines for Coated Tablets

Posted on March 3, 2025 By Admin

Addressing Cross-Contamination Risks in Shared Utility Lines for Coated Tablets Addressing Cross-Contamination Risks in Shared Utility Lines for Coated Tablets Introduction: In the pharmaceutical industry, maintaining product integrity and patient safety is paramount. One of the significant challenges faced by manufacturers is the risk of cross-contamination, especially when utilizing shared utility lines for coated tablets….

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Solid Dosage form, Tablets

Addressing Non-Uniform Coating Thickness in Sugar-Coated Tablets

Posted on March 3, 2025 By Admin

Addressing Non-Uniform Coating Thickness in Sugar-Coated Tablets Addressing Non-Uniform Coating Thickness in Sugar-Coated Tablets Introduction: Sugar-coated tablets are a time-tested pharmaceutical dosage form, favored for their aesthetic appeal, masking of unpleasant tastes, and protection of the core tablet. Achieving a uniformly coated product is critical not only for consumer acceptance but also for ensuring consistent…

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Solid Dosage form, Tablets

Managing Failures in Batch Sampling for Quality Assurance

Posted on March 2, 2025 By Admin

Managing Failures in Batch Sampling for Quality Assurance Managing Failures in Batch Sampling for Quality Assurance Introduction: In the pharmaceutical industry, ensuring the quality of a product is paramount. Batch sampling plays a critical role in this process, providing a snapshot that represents the entire production batch. However, managing failures in batch sampling is crucial…

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Solid Dosage form, Tablets

Inadequate systems for monitoring microbial control in water systems.

Posted on March 2, 2025 By Admin

Inadequate systems for monitoring microbial control in water systems. Inadequate systems for monitoring microbial control in water systems. Introduction: In the pharmaceutical industry, water is a critical component used in various stages of drug manufacturing, from formulation to cleaning processes. Ensuring the microbiological quality of water is paramount, as inadequate systems for monitoring microbial control…

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

Addressing Coating Delamination Issues During In-Process Quality Checks

Posted on March 2, 2025 By Admin

Addressing Coating Delamination Issues During In-Process Quality Checks Addressing Coating Delamination Issues During In-Process Quality Checks Introduction: In the pharmaceutical industry, tablets are one of the most common solid dosage forms. The coating of these tablets plays a pivotal role not only in aesthetics but also in functionality, including protection from environmental conditions, masking taste,…

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Solid Dosage form, Tablets

Resolving Weight Variation Failures in Bilayer Tablets

Posted on March 2, 2025 By Admin

Resolving Weight Variation Failures in Bilayer Tablets Resolving Weight Variation Failures in Bilayer Tablets Introduction: In the pharmaceutical industry, bilayer tablets have emerged as a sophisticated solution for delivering multiple drugs or achieving different release profiles in a single dosage form. However, maintaining uniform weight across these tablets poses significant challenges, impacting quality and efficacy….

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Solid Dosage form, Tablets

Ensuring Compliance with GMP Standards in Utility Validation Documentation

Posted on March 1, 2025 By Admin

Ensuring Compliance with GMP Standards in Utility Validation Documentation Ensuring Compliance with GMP Standards in Utility Validation Documentation Introduction: The pharmaceutical industry operates under strict regulations to ensure the safety, quality, and efficacy of products. Good Manufacturing Practice (GMP) standards are integral to these regulations, guiding the production, testing, and quality assurance of pharmaceutical products….

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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

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

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

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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