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Tag: Quality control

Addressing Problems in Tamper-Evident Sealing for Enteric-Coated Tablets

Posted on May 17, 2025 By Admin

Addressing Problems in Tamper-Evident Sealing for Enteric-Coated Tablets Addressing Problems in Tamper-Evident Sealing for Enteric-Coated Tablets Introduction: In the pharmaceutical industry, ensuring the safety and integrity of drug products is paramount. Enteric-coated tablets are designed to withstand the acidic environment of the stomach and dissolve in the more neutral pH of the intestine, providing targeted…

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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

Validating Rinse Volume Requirements in Cleaning Validation Protocols

Posted on May 15, 2025 By Admin

Validating Rinse Volume Requirements in Cleaning Validation Protocols Validating Rinse Volume Requirements in Cleaning Validation Protocols Introduction: In the pharmaceutical industry, ensuring that manufacturing equipment is free from contaminants is paramount to product safety and efficacy. Cleaning validation is a critical component of Good Manufacturing Practice (GMP) to confirm that cleaning processes are effective and…

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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

Ensuring Consistency in Hardness Testing During Validation of Compression Lines

Posted on May 11, 2025 By Admin

Ensuring Consistency in Hardness Testing During Validation of Compression Lines Ensuring Consistency in Hardness Testing During Validation of Compression Lines Introduction: The pharmaceutical industry places a significant emphasis on the quality and consistency of solid dosage forms, particularly tablets. Tablet hardness is a critical quality attribute that influences not only the tablet’s mechanical strength but…

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Solid Dosage form, Tablets

Investigating API Potency Retention in Immediate Release Tablets Over Time

Posted on May 11, 2025 By Admin

Investigating API Potency Retention in Immediate Release Tablets Over Time Investigating API Potency Retention in Immediate Release Tablets Over Time Introduction: In the pharmaceutical industry, ensuring the efficacy and safety of medicinal products is paramount. One critical aspect of this is the potency retention of the Active Pharmaceutical Ingredient (API) in immediate release tablets over…

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Solid Dosage form, Tablets

Troubleshooting Calibration Failures in Dissolution Testing Equipment

Posted on May 10, 2025 By Admin

Troubleshooting Calibration Failures in Dissolution Testing Equipment Troubleshooting Calibration Failures in Dissolution Testing Equipment Introduction: Dissolution testing is a critical process in the pharmaceutical industry, serving as a quality control measure to ensure the efficacy and safety of tablets and other solid dosage forms. Calibration of dissolution testing equipment is essential for accurate and reliable…

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Solid Dosage form, Tablets

Validating Rinse Water Analysis for Cleaning Validation in Sugar-Coating Processes

Posted on May 9, 2025 By Admin

Validating Rinse Water Analysis for Cleaning Validation in Sugar-Coating Processes Validating Rinse Water Analysis for Cleaning Validation in Sugar-Coating Processes Introduction: In the pharmaceutical industry, maintaining stringent cleanliness standards is paramount, particularly in processes involving solid dosage forms like tablets. Sugar-coating, a prevalent method for enhancing tablet aesthetics and masking unpleasant tastes, involves multiple stages…

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Solid Dosage form, Tablets

Managing Documentation Deviations in Process Validation Protocols

Posted on May 7, 2025 By Admin

Managing Documentation Deviations in Process Validation Protocols Managing Documentation Deviations in Process Validation Protocols Introduction: In the pharmaceutical industry, process validation is a critical component of ensuring product quality and compliance with regulatory standards. It involves a series of documented procedures and protocols designed to confirm that a manufacturing process consistently produces a product meeting…

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Solid Dosage form, Tablets

Ensuring Robustness in QA Monitoring for Immediate Release Tablets

Posted on May 5, 2025 By Admin

Ensuring Robustness in QA Monitoring for Immediate Release Tablets Ensuring Robustness in QA Monitoring for Immediate Release Tablets Introduction: Quality Assurance (QA) in the pharmaceutical industry is a critical component that ensures the safety, efficacy, and quality of medicinal products. For immediate release tablets, which are designed to disintegrate and release their active pharmaceutical ingredients…

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Solid Dosage form, Tablets

Managing Documentation Errors During QA Audits for Coated Tablets

Posted on May 5, 2025 By Admin

Managing Documentation Errors During QA Audits for Coated Tablets Managing Documentation Errors During QA Audits for Coated Tablets Introduction: In the pharmaceutical industry, maintaining rigorous quality assurance (QA) standards is critical, particularly during the production of coated tablets. These solid dosage forms are widely used, and their efficacy and safety hinge on meticulous manufacturing processes…

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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

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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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