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Tag: pharmaceutical quality assurance]

Addressing Brittleness in Sugar-Coated Tablets During Validation Studies

Posted on May 25, 2025 By Admin

Addressing Brittleness in Sugar-Coated Tablets During Validation Studies Addressing Brittleness in Sugar-Coated Tablets During Validation Studies Introduction: Sugar-coated tablets have long been a popular choice in pharmaceutical manufacturing due to their aesthetic appeal, ease of swallowing, and ability to mask the taste of active ingredients. However, the process of sugar coating can introduce brittleness, posing…

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Solid Dosage form, Tablets

Troubleshooting Powder Segregation Issues During Validation of Compression Lines

Posted on May 25, 2025 By Admin

Troubleshooting Powder Segregation Issues During Validation of Compression Lines Troubleshooting Powder Segregation Issues During Validation of Compression Lines Introduction: In the realm of pharmaceutical manufacturing, maintaining the uniformity and consistency of solid dosage forms, such as tablets, is crucial. One of the common challenges faced during the validation of compression lines is powder segregation. This…

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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 Non-Uniform Granule Size in Fluid Bed Granulators During Validation

Posted on May 20, 2025 By Admin

Addressing Non-Uniform Granule Size in Fluid Bed Granulators During Validation Addressing Non-Uniform Granule Size in Fluid Bed Granulators During Validation Introduction: In the pharmaceutical industry, maintaining consistent granule size during the fluid bed granulation process is crucial for ensuring the quality and efficacy of solid dosage forms like tablets. Granule size uniformity affects the flow…

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Solid Dosage form, Tablets

Resolving Tablet Positioning Issues in Blister Cavity Formation

Posted on May 20, 2025 By Admin

Resolving Tablet Positioning Issues in Blister Cavity Formation Resolving Tablet Positioning Issues in Blister Cavity Formation Introduction: In the pharmaceutical industry, blister packaging is a critical aspect of product presentation and protection. Tablets must be securely and accurately positioned within blister cavities to ensure product stability, compliance, and consumer safety. Misalignment or improper positioning can…

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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

Addressing Non-Compliance in QA Tests for Multi-Layer Tablets

Posted on May 16, 2025 By Admin

Addressing Non-Compliance in QA Tests for Multi-Layer Tablets Addressing Non-Compliance in QA Tests for Multi-Layer Tablets Introduction: In the pharmaceutical industry, multi-layer tablets have emerged as a preferred solid dosage form due to their ability to deliver multiple active pharmaceutical ingredients (APIs) in a single dose and to provide controlled release of medications. However, ensuring…

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Solid Dosage form, Tablets

Troubleshooting Failures in Acid Resistance Testing of Enteric-Coated Tablets

Posted on May 12, 2025 By Admin

Troubleshooting Failures in Acid Resistance Testing of Enteric-Coated Tablets Troubleshooting Failures in Acid Resistance Testing of Enteric-Coated Tablets Introduction: Enteric-coated tablets are a critical part of modern pharmacology, designed to protect active ingredients from the acidic environment of the stomach and ensure release in the more neutral pH of the intestine. This targeted delivery system…

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Solid Dosage form, Tablets

Managing Layer Delamination Issues in Multi-Layer Tablets During Validation

Posted on May 12, 2025 By Admin

Managing Layer Delamination Issues in Multi-Layer Tablets During Validation Managing Layer Delamination Issues in Multi-Layer Tablets During Validation Introduction: In the pharmaceutical industry, multi-layer tablets are a popular dosage form due to their ability to deliver multiple drugs or distinct release profiles in a single tablet. However, manufacturing such tablets comes with its own set…

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Solid Dosage form, Tablets

Addressing Cross-Contamination Risks in Shared Tablet Manufacturing Equipment

Posted on May 5, 2025 By Admin

Addressing Cross-Contamination Risks in Shared Tablet Manufacturing Equipment Addressing Cross-Contamination Risks in Shared Tablet Manufacturing Equipment Introduction: In the pharmaceutical industry, ensuring the safety and efficacy of drug products is paramount. With the increasing demand for diverse medications, many manufacturers utilize shared equipment for tablet production to optimize resources. However, shared equipment can pose significant…

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Solid Dosage form, Tablets

Challenges in achieving uniform capsule transparency during validation.

Posted on May 3, 2025 By Admin

Challenges in achieving uniform capsule transparency during validation. Challenges in achieving uniform capsule transparency during validation. Introduction: In the pharmaceutical industry, the demand for consistent and high-quality solid oral dosage forms has never been greater. Among these, capsules, particularly hard and soft gelatin capsules, stand out due to their versatility and consumer preference for ease…

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

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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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