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Tips for: Tablets

Validating Cleanroom Classification for Sustained Release Tablet Manufacturing Facilities

Posted on March 1, 2025 By Admin

The pharmaceutical industry is heavily reliant on maintaining controlled environments to ensure the safety and efficacy of its products. Cleanrooms play a critical role in the manufacturing of pharmaceutical products, particularly for sustained release tablets, where environmental control can directly impact product quality. This article delves into the complexities of validating cleanroom classification in the context of sustained release tablet manufacturing, highlighting the importance of adhering to strict regulatory standards and implementing effective contamination control strategies.
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Solid Dosage form, Tablets

Troubleshooting Uneven Spray Patterns During Coating Process Validation

Posted on March 1, 2025 By Admin

In the realm of pharmaceutical manufacturing, ensuring uniform coating of tablets is vital for both aesthetic appeal and functional efficacy. Coating serves multiple purposes, including protection from environmental conditions, masking taste, and controlling the release of active pharmaceutical ingredients (APIs). An uneven spray pattern during the coating process can lead to significant quality issues, impacting the product’s effectiveness and regulatory compliance. This guide delves into troubleshooting techniques for addressing uneven spray patterns during coating process validation, ensuring optimal product quality and adherence to industry standards.
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Solid Dosage form, Tablets

Preventing Layer Separation in Multi-Layer Tablet Designs

Posted on March 1, 2025 By Admin

In the realm of pharmaceutical manufacturing, multi-layer tablets offer a sophisticated solution for delivering multiple active pharmaceutical ingredients (APIs) with distinct release profiles. However, this complexity introduces the critical challenge of preventing layer separation, a phenomenon that can compromise tablet integrity, efficacy, and patient safety. Ensuring cohesive and stable multi-layer tablets is essential for maintaining therapeutic consistency and meeting stringent regulatory standards.
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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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