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Tag: Tablet Testing]

Troubleshooting Failures in Stability Testing for Film-Coated Tablets

Posted on March 30, 2025 By Admin

Troubleshooting Failures in Stability Testing for Film-Coated Tablets Troubleshooting Failures in Stability Testing for Film-Coated Tablets Introduction: Stability testing is a critical component in the lifecycle of any pharmaceutical product, especially for film-coated tablets. These tests ensure that the product maintains its intended efficacy, safety, and quality throughout its shelf life. Stability testing evaluates how…

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Solid Dosage form, Tablets

Managing Over-Compression in Tablets Prone to Brittleness

Posted on March 30, 2025 By Admin

Managing Over-Compression in Tablets Prone to Brittleness Managing Over-Compression in Tablets Prone to Brittleness Introduction: In the pharmaceutical industry, tablet formulation and manufacturing are critical processes that ensure medication efficacy and patient safety. Among the numerous challenges faced in tablet production, managing over-compression in tablets prone to brittleness stands out. Over-compression can lead to brittle…

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Solid Dosage form, Tablets

Ensuring Consistency in Batch-to-Batch Content Uniformity for Tablets

Posted on March 30, 2025 By Admin

Ensuring Consistency in Batch-to-Batch Content Uniformity for Tablets Ensuring Consistency in Batch-to-Batch Content Uniformity for Tablets Introduction: In the pharmaceutical industry, ensuring consistency in batch-to-batch content uniformity of tablets is paramount. Content uniformity is crucial for maintaining the safety and efficacy of medications. Variability in the active pharmaceutical ingredient (API) distribution can lead to suboptimal…

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Solid Dosage form, Tablets

Root Cause Analysis of Failures in Weight Uniformity Tests

Posted on March 26, 2025 By Admin

Root Cause Analysis of Failures in Weight Uniformity Tests Root Cause Analysis of Failures in Weight Uniformity Tests Introduction: In the realm of pharmaceutical manufacturing, ensuring the consistency and quality of dosage forms is paramount. One of the critical quality control tests for solid dosage forms, specifically tablets, is the weight uniformity test. This test…

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Solid Dosage form, Tablets

Troubleshooting Thickness Testing Failures in Enteric-Coated Tablets

Posted on March 26, 2025 By Admin

Troubleshooting Thickness Testing Failures in Enteric-Coated Tablets Troubleshooting Thickness Testing Failures in Enteric-Coated Tablets Introduction: Enteric-coated tablets are a critical component in the pharmaceutical industry, designed to deliver active ingredients to the intestines without being degraded by stomach acid. The integrity of this enteric coating is vital, and one key quality parameter is the thickness…

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Solid Dosage form, Tablets

Troubleshooting Dissolution Failures in Enteric-Coated Tablets

Posted on March 24, 2025 By Admin

Troubleshooting Dissolution Failures in Enteric-Coated Tablets Troubleshooting Dissolution Failures in Enteric-Coated Tablets Introduction: Enteric-coated tablets are a sophisticated pharmaceutical dosage form designed to bypass the acidic environment of the stomach and dissolve in the more neutral pH of the intestines. This coating is crucial for drugs that can be degraded by stomach acid or can…

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Solid Dosage form, Tablets

Ensuring Adequate pH Stability in Enteric-Coated Tablets During Testing

Posted on March 22, 2025 By Admin

Ensuring Adequate pH Stability in Enteric-Coated Tablets During Testing Ensuring Adequate pH Stability in Enteric-Coated Tablets During Testing Introduction: In the pharmaceutical industry, enteric-coated tablets play a crucial role in ensuring that active pharmaceutical ingredients (APIs) are delivered to the intestine, bypassing the acidic environment of the stomach. This not only protects the drug from…

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Solid Dosage form, Tablets

Troubleshooting Brittleness Failures in Immediate Release Tablets

Posted on March 21, 2025 By Admin

Troubleshooting Brittleness Failures in Immediate Release Tablets Troubleshooting Brittleness Failures in Immediate Release Tablets Introduction: Immediate release tablets represent a significant portion of the pharmaceutical market due to their convenience and effectiveness in delivering medication rapidly. However, brittleness failures in these tablets can pose substantial challenges, affecting their integrity and therapeutic efficacy. Brittleness, often resulting…

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Solid Dosage form, Tablets

Identifying Root Causes of Poor Disintegration in Film-Coated Tablets

Posted on March 21, 2025 By Admin

Identifying Root Causes of Poor Disintegration in Film-Coated Tablets Identifying Root Causes of Poor Disintegration in Film-Coated Tablets Introduction: Film-coated tablets are a popular solid dosage form in the pharmaceutical industry due to their enhanced stability, ease of ingestion, and ability to mask unpleasant tastes. However, one critical quality attribute for these tablets is their…

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Solid Dosage form, Tablets

Identifying Causes of Tablet Swelling During Disintegration Testing

Posted on March 17, 2025 By Admin

Identifying Causes of Tablet Swelling During Disintegration Testing Identifying Causes of Tablet Swelling During Disintegration Testing Introduction: In the pharmaceutical industry, ensuring the quality and efficacy of solid dosage forms, such as tablets, is paramount. A critical aspect of this quality control is disintegration testing, a process that evaluates how quickly a tablet breaks down…

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Solid Dosage form, Tablets

Addressing Challenges in Friability Testing for High-Speed Compression Tablets

Posted on March 17, 2025 By Admin

Addressing Challenges in Friability Testing for High-Speed Compression Tablets Addressing Challenges in Friability Testing for High-Speed Compression Tablets Introduction: In the pharmaceutical industry, tablets remain one of the most common dosage forms due to their convenience, stability, and ease of administration. However, ensuring the integrity and quality of tablets, especially those produced at high speed,…

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Solid Dosage form, Tablets

Ensuring Consistency in Dissolution Testing for Multi-API Tablets

Posted on March 16, 2025 By Admin

Ensuring Consistency in Dissolution Testing for Multi-API Tablets Ensuring Consistency in Dissolution Testing for Multi-API Tablets Introduction: Dissolution testing is a critical quality control measure in the pharmaceutical industry, particularly for tablets containing multiple active pharmaceutical ingredients (APIs). Ensuring consistency in dissolution testing is vital as it impacts the tablet’s efficacy, safety, and regulatory compliance….

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Solid Dosage form, Tablets

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  • Aerosol Formulations
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  • 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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