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Tag: Tablet Formulation Challenges

Ensuring Consistent Release Profiles in Multi-API Tablets Over Time

Posted on May 27, 2025 By Admin

Ensuring Consistent Release Profiles in Multi-API Tablets Over Time Ensuring Consistent Release Profiles in Multi-API Tablets Over Time Introduction: In the pharmaceutical industry, the formulation and manufacturing of multi-API (Active Pharmaceutical Ingredient) tablets present a complex challenge. Ensuring consistent drug release profiles over time is crucial for therapeutic efficacy and patient safety. A consistent release…

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Solid Dosage form, Tablets

Ensuring Adequate Process Controls for Hygroscopic Tablet Production

Posted on May 14, 2025 By Admin

Ensuring Adequate Process Controls for Hygroscopic Tablet Production Ensuring Adequate Process Controls for Hygroscopic Tablet Production Introduction: Hygroscopic tablets, known for their ability to absorb moisture from the environment, pose unique challenges in pharmaceutical manufacturing. Ensuring adequate process controls during their production is crucial for maintaining product stability, efficacy, and quality. This comprehensive guide delves…

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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

Ensuring Robustness of Coating Adhesion in Multi-API Tablets Over Time

Posted on May 4, 2025 By Admin

Ensuring Robustness of Coating Adhesion in Multi-API Tablets Over Time Ensuring Robustness of Coating Adhesion in Multi-API Tablets Over Time Introduction: In the dynamic landscape of pharmaceutical manufacturing, ensuring the robustness of coating adhesion in multi-API (Active Pharmaceutical Ingredient) tablets is crucial. The coating plays a pivotal role in protecting the drug, controlling its release,…

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Solid Dosage form, Tablets

Troubleshooting Residual Solvent Issues in Film-Coated Tablets During Validation

Posted on April 16, 2025 By Admin

Troubleshooting Residual Solvent Issues in Film-Coated Tablets During Validation Troubleshooting Residual Solvent Issues in Film-Coated Tablets During Validation Introduction: The pharmaceutical industry is highly regulated, with stringent guidelines ensuring that products are safe and effective for consumers. Among the numerous challenges faced by manufacturers is the control of residual solvents in film-coated tablets. These solvents,…

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Solid Dosage form, Tablets

Investigating Core Erosion in Extended Release Tablets During Stability Storage

Posted on April 13, 2025 By Admin

Investigating Core Erosion in Extended Release Tablets During Stability Storage Investigating Core Erosion in Extended Release Tablets During Stability Storage Introduction: In the realm of pharmaceutical development, extended release (ER) tablets play a pivotal role in ensuring patient compliance and therapeutic efficacy. These tablets are designed to release active pharmaceutical ingredients (APIs) at a controlled…

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Solid Dosage form, Tablets

Ensuring Batch-to-Batch Consistency in Weight Variation Validation

Posted on April 10, 2025 By Admin

Ensuring Batch-to-Batch Consistency in Weight Variation Validation Ensuring Batch-to-Batch Consistency in Weight Variation Validation Introduction: In the pharmaceutical industry, ensuring the consistency and quality of tablet production is paramount. Weight variation validation is a critical component in the manufacturing process of solid dosage forms, particularly tablets. It ensures that each tablet in a batch contains…

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Solid Dosage form, Tablets

Addressing Over-Drying in Sugar-Coated Tablets During Curing

Posted on March 27, 2025 By Admin

Addressing Over-Drying in Sugar-Coated Tablets During Curing Addressing Over-Drying in Sugar-Coated Tablets During Curing Introduction: Sugar-coating is an essential phase in the production of tablets, offering not only aesthetic appeal but also protection from environmental factors. However, one of the prevalent challenges during the sugar-coating process is over-drying, which can compromise the integrity and effectiveness…

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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

Addressing Brittleness in High-Compression Tablets During Stability Studies

Posted on March 21, 2025 By Admin

Addressing Brittleness in High-Compression Tablets During Stability Studies Addressing Brittleness in High-Compression Tablets During Stability Studies Introduction: In the pharmaceutical industry, the development and production of solid dosage forms, particularly tablets, is a critical aspect of delivering effective therapies to patients. High-compression tablets are increasingly popular due to their compact size and ease of production….

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Solid Dosage form, Tablets

Managing Variability in Dissolution Testing for Immediate Release Tablets

Posted on March 16, 2025 By Admin

Managing Variability in Dissolution Testing for Immediate Release Tablets Managing Variability in Dissolution Testing for Immediate Release Tablets Introduction: Dissolution testing is a critical quality control measure in the pharmaceutical industry, particularly for immediate release tablets. This test ensures that the tablet releases its active ingredients at the desired rate and extent, which is crucial…

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Solid Dosage form, Tablets

Common Dissolution Failures in Immediate Release Tablets

Posted on March 9, 2025 By Admin

Common Dissolution Failures in Immediate Release Tablets Common Dissolution Failures in Immediate Release Tablets Introduction: Immediate release tablets are a cornerstone of oral pharmaceutical dosage forms, designed to disintegrate and release their active ingredients promptly upon ingestion. The dissolution process plays a critical role in ensuring the therapeutic efficacy and bioavailability of these tablets. However,…

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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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