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Tag: pharmaceutical compliance

Resolving Challenges in Handling Soft Gel Tablets During Packaging

Posted on March 22, 2025 By Admin

Resolving Challenges in Handling Soft Gel Tablets During Packaging Resolving Challenges in Handling Soft Gel Tablets During Packaging Introduction: Soft gel tablets, often referred to as soft gelatin capsules, are a popular dosage form in the pharmaceutical industry, valued for their ease of swallowing, ability to mask unpleasant tastes, and capability to deliver liquid or…

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Solid Dosage form, Tablets

Investigating Failures in Dissolution Testing for Sustained Release Tablets

Posted on March 22, 2025 By Admin

Investigating Failures in Dissolution Testing for Sustained Release Tablets Investigating Failures in Dissolution Testing for Sustained Release Tablets Introduction: The pharmaceutical industry is a cornerstone of modern medicine, with sustained release tablets playing a crucial role in controlled drug delivery systems. These formulations are designed to release the active pharmaceutical ingredient (API) at a predetermined…

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Solid Dosage form, Tablets

Addressing Failures in Temperature Uniformity for Steam Quality Testing

Posted on March 22, 2025 By Admin

Addressing Failures in Temperature Uniformity for Steam Quality Testing Addressing Failures in Temperature Uniformity for Steam Quality Testing Introduction: In the pharmaceutical industry, ensuring the sterility of products is paramount, and autoclaves play a critical role in this process. Steam quality testing, particularly temperature uniformity, is a vital component in validating the efficacy of the…

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Solid Dosage form, Tablets

Managing Packing Material Variation for Consistency in Blister Packaging

Posted on March 21, 2025 By Admin

Managing Packing Material Variation for Consistency in Blister Packaging Managing Packing Material Variation for Consistency in Blister Packaging Introduction: In the pharmaceutical industry, blister packaging serves as a critical component for ensuring the stability and protection of solid dosage forms like tablets. The packaging not only safeguards the medication but also ensures patient compliance and…

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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

Ensuring Adherence to GMP Standards in Documentation for QA Processes

Posted on March 20, 2025 By Admin

Ensuring Adherence to GMP Standards in Documentation for QA Processes Ensuring Adherence to GMP Standards in Documentation for QA Processes Introduction: In the world of pharmaceutical manufacturing, ensuring the quality and safety of products is paramount. This is where Good Manufacturing Practice (GMP) standards come into play, serving as a cornerstone for quality assurance (QA)…

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Solid Dosage form, Tablets

Challenges in maintaining proper documentation for vendor qualification.

Posted on March 20, 2025 By Admin

Challenges in maintaining proper documentation for vendor qualification. Challenges in maintaining proper documentation for vendor qualification Introduction: In the pharmaceutical industry, vendor qualification is a critical component of ensuring product quality and safety. Proper documentation is not just a regulatory requirement but also a fundamental practice to maintain a reliable and efficient supply chain. Vendor…

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

Addressing Over-Sensitivity to Humidity in Hygroscopic Tablets

Posted on March 19, 2025 By Admin

Addressing Over-Sensitivity to Humidity in Hygroscopic Tablets Addressing Over-Sensitivity to Humidity in Hygroscopic Tablets Introduction: In the pharmaceutical industry, the stability of solid dosage forms like tablets is paramount to ensuring efficacy and safety. Hygroscopic tablets, which readily absorb moisture from their environment, present unique challenges in terms of formulation, manufacturing, and storage. Over-sensitivity to…

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Solid Dosage form, Tablets

Addressing Granule Segregation During Roller Compaction

Posted on March 19, 2025 By Admin

Addressing Granule Segregation During Roller Compaction Addressing Granule Segregation During Roller Compaction Introduction: In the realm of pharmaceutical manufacturing, ensuring the uniformity and quality of solid dosage forms such as tablets is crucial. Roller compaction is a dry granulation process commonly used to improve the flow properties and compressibility of powders. However, one of the…

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Solid Dosage form, Tablets

Common Issues in Batch Sampling for Quality Testing of Tablets

Posted on March 19, 2025 By Admin

Common Issues in Batch Sampling for Quality Testing of Tablets Common Issues in Batch Sampling for Quality Testing of Tablets Introduction: In the pharmaceutical industry, ensuring the quality and efficacy of tablet batches is paramount. Batch sampling is a critical process that involves selecting a representative sample from a production batch to assess the quality…

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Solid Dosage form, Tablets

Ensuring Consistency in Content Uniformity Tests Across Batches

Posted on March 19, 2025 By Admin

Ensuring Consistency in Content Uniformity Tests Across Batches Ensuring Consistency in Content Uniformity Tests Across Batches Introduction: In the pharmaceutical industry, the consistency of content uniformity tests across batches is pivotal to ensuring the safety and efficacy of solid dosage forms, particularly tablets. Content uniformity is a critical quality attribute that determines whether each tablet…

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Solid Dosage form, Tablets

High variability in documentation practices for batch records.

Posted on March 18, 2025 By Admin

High variability in documentation practices for batch records. High Variability in Documentation Practices for Batch Records Introduction: In the pharmaceutical industry, maintaining precise and consistent documentation practices for batch records is critical. These records serve as the blueprint of manufacturing processes, ensuring that each batch of product meets stringent quality standards. However, high variability in…

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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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