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Tag: Tablet formulation

Managing Deviations in Batch Records for Enteric-Coated Tablets

Posted on May 9, 2025 By Admin

Managing Deviations in Batch Records for Enteric-Coated Tablets Managing Deviations in Batch Records for Enteric-Coated Tablets Introduction: In the pharmaceutical industry, maintaining the integrity of batch records is crucial for ensuring the quality and compliance of drug products. Enteric-coated tablets, designed to withstand the acidic environment of the stomach and dissolve in the more neutral…

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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

Managing Adhesion Failures in Sustained Release Tablet Coating Layers During Validation

Posted on May 5, 2025 By Admin

Managing Adhesion Failures in Sustained Release Tablet Coating Layers During Validation Managing Adhesion Failures in Sustained Release Tablet Coating Layers During Validation Introduction: Sustained release tablets are a cornerstone in modern pharmaceutical delivery systems, designed to release their active ingredient gradually over time to maintain therapeutic levels in the bloodstream. The coating on these tablets…

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Solid Dosage form, Tablets

Ensuring Consistency in Granule Size Distribution During Validation Testing

Posted on May 4, 2025 By Admin

Ensuring Consistency in Granule Size Distribution During Validation Testing Ensuring Consistency in Granule Size Distribution During Validation Testing Introduction: In the pharmaceutical industry, ensuring consistency in granule size distribution during validation testing is crucial for the production of high-quality solid dosage forms, particularly tablets. Granule size directly influences the flowability, compressibility, and dissolution rates of…

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Solid Dosage form, Tablets

Ensuring Packaging Compatibility for Tablets with Extended Stability Requirements

Posted on May 4, 2025 By Admin

Ensuring Packaging Compatibility for Tablets with Extended Stability Requirements Ensuring Packaging Compatibility for Tablets with Extended Stability Requirements Introduction: In the pharmaceutical industry, ensuring the stability and efficacy of tablets throughout their shelf life is paramount. This is particularly critical for tablets with extended stability requirements. The compatibility between the packaging and the tablet formulation…

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Solid Dosage form, Tablets

Managing Surface Erosion in Sugar-Coated Tablets During Stability Studies

Posted on May 3, 2025 By Admin

Managing Surface Erosion in Sugar-Coated Tablets During Stability Studies Managing Surface Erosion in Sugar-Coated Tablets During Stability Studies Introduction: In the pharmaceutical industry, sugar-coated tablets have been a popular choice for delivering active pharmaceutical ingredients (APIs) due to their aesthetic appeal, ease of swallowing, and ability to mask the taste of certain drugs. However, during…

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Solid Dosage form, Tablets

Troubleshooting Poor Coating Adhesion in Extended Release Tablets Over Time

Posted on May 3, 2025 By Admin

Troubleshooting Poor Coating Adhesion in Extended Release Tablets Over Time Troubleshooting Poor Coating Adhesion in Extended Release Tablets Over Time Introduction: Extended release tablets are a crucial aspect of modern pharmaceutical delivery systems, offering consistent therapeutic effects over extended periods. However, the integrity of their coating is paramount to ensure proper drug release and efficacy….

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Solid Dosage form, Tablets

Ensuring Consistency in Disintegration Time During Long-Term Stability Studies

Posted on May 3, 2025 By Admin

Ensuring Consistency in Disintegration Time During Long-Term Stability Studies Ensuring Consistency in Disintegration Time During Long-Term Stability Studies Introduction: In the realm of pharmaceuticals, ensuring consistency in the disintegration time of tablets during long-term stability studies is pivotal for guaranteeing a drug’s efficacy, safety, and patient compliance. Disintegration time is a critical quality attribute that…

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Solid Dosage form, Tablets

Managing API Degradation in Film-Coated Tablets Stored at High Temperatures

Posted on May 1, 2025 By Admin

Managing API Degradation in Film-Coated Tablets Stored at High Temperatures Managing API Degradation in Film-Coated Tablets Stored at High Temperatures Introduction: In the pharmaceutical industry, the stability of Active Pharmaceutical Ingredients (APIs) is crucial for ensuring the efficacy and safety of medications. Film-coated tablets are a popular dosage form, offering benefits such as ease of…

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Solid Dosage form, Tablets

Investigating Non-Uniform Dissolution in Enteric-Coated Tablets During Testing

Posted on April 30, 2025 By Admin

Investigating Non-Uniform Dissolution in Enteric-Coated Tablets During Testing Investigating Non-Uniform Dissolution in Enteric-Coated Tablets During Testing Introduction: The pharmaceutical industry constantly strives to develop effective drug delivery mechanisms, with enteric-coated tablets serving as a crucial form of solid dosage. These tablets are designed to resist the acidic environment of the stomach, releasing their active ingredients…

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Solid Dosage form, Tablets

Troubleshooting Surface Roughness in Sugar-Coated Tablets During Storage

Posted on April 30, 2025 By Admin

Troubleshooting Surface Roughness in Sugar-Coated Tablets During Storage Troubleshooting Surface Roughness in Sugar-Coated Tablets During Storage Introduction: Sugar-coated tablets are a prevalent form of oral pharmaceutical dosage due to their aesthetic appeal, taste masking abilities, and protective properties. However, during storage, these tablets can sometimes develop surface roughness, which can compromise their appearance, consumer acceptance,…

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Solid Dosage form, Tablets

Addressing Deviations in Stability Studies for Bilayer Tablets

Posted on April 27, 2025 By Admin

Addressing Deviations in Stability Studies for Bilayer Tablets Addressing Deviations in Stability Studies for Bilayer Tablets Introduction: Bilayer tablets have emerged as a versatile drug delivery system, offering the advantage of combining two different drugs or formulations with varied release profiles in a single dosage form. This innovation not only improves patient compliance but also…

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Solid Dosage form, Tablets

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  • Aerosol Formulations
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  • 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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