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Tag: Pharmaceutical Industry

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

Addressing Non-Compliance in Stability Studies for Film-Coated Tablets

Posted on March 20, 2025 By Admin

Addressing Non-Compliance in Stability Studies for Film-Coated Tablets Addressing Non-Compliance in Stability Studies for Film-Coated Tablets Introduction: In the pharmaceutical industry, stability studies play a crucial role in ensuring the efficacy, safety, and quality of drug products. For film-coated tablets, stability studies are essential to evaluate how the product maintains its intended physical, chemical, microbiological,…

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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

Preventing Powder Loss During Tablet Compression

Posted on March 18, 2025 By Admin

Preventing Powder Loss During Tablet Compression Preventing Powder Loss During Tablet Compression Introduction: Tablet compression is a critical process in pharmaceutical manufacturing, responsible for converting powder into solid dosage forms like tablets. Ensuring efficiency during this process is vital for maintaining product quality, consistency, and cost-effectiveness. Powder loss during tablet compression can lead to significant…

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Solid Dosage form, Tablets

Ensuring Adequacy of Humidity Control Systems for Sugar-Coated Tablet Areas

Posted on March 18, 2025 By Admin

Ensuring Adequacy of Humidity Control Systems for Sugar-Coated Tablet Areas Ensuring Adequacy of Humidity Control Systems for Sugar-Coated Tablet Areas Introduction: In the pharmaceutical industry, maintaining precise environmental conditions is crucial for the manufacturing of high-quality products. Specifically, the production of sugar-coated tablets requires stringent humidity control to ensure the integrity and efficacy of the…

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Solid Dosage form, Tablets

High variability in content uniformity testing for multi-drug capsules.

Posted on March 18, 2025 By Admin

High variability in content uniformity testing for multi-drug capsules. High Variability in Content Uniformity Testing for Multi-Drug Capsules Introduction: Content uniformity is a critical quality attribute in the manufacturing of pharmaceuticals, ensuring that each dose in a batch contains the intended amount of active pharmaceutical ingredients (APIs). In the context of multi-drug capsules, achieving content…

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

Managing Fines Generation During Compression of Immediate Release Tablets

Posted on March 17, 2025 By Admin

Managing Fines Generation During Compression of Immediate Release Tablets Managing Fines Generation During Compression of Immediate Release Tablets Introduction: In the pharmaceutical industry, the production of immediate-release tablets is a crucial process that requires meticulous attention to detail. One of the significant challenges faced during the tablet manufacturing process is the generation of fines. Fines…

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Solid Dosage form, Tablets

Identifying Causes of Tablet Swelling During Disintegration Testing

Posted on March 17, 2025 By Admin

Identifying Causes of Tablet Swelling During Disintegration Testing Identifying Causes of Tablet Swelling During Disintegration Testing Introduction: In the pharmaceutical industry, ensuring the quality and efficacy of solid dosage forms, such as tablets, is paramount. A critical aspect of this quality control is disintegration testing, a process that evaluates how quickly a tablet breaks down…

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Solid Dosage form, Tablets

Troubleshooting Uneven Color Distribution in Sugar-Coated Tablets

Posted on March 17, 2025 By Admin

Troubleshooting Uneven Color Distribution in Sugar-Coated Tablets Troubleshooting Uneven Color Distribution in Sugar-Coated Tablets Introduction: Sugar-coated tablets are a popular dosage form in the pharmaceutical industry due to their ability to mask unpleasant tastes and improve patient compliance. However, achieving a uniform color distribution on these tablets can be challenging. Uneven color distribution not only…

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Solid Dosage form, Tablets

Troubleshooting Non-Homogeneous Color Distribution in Sugar-Coated Tablets

Posted on March 17, 2025 By Admin

Troubleshooting Non-Homogeneous Color Distribution in Sugar-Coated Tablets Troubleshooting Non-Homogeneous Color Distribution in Sugar-Coated Tablets Introduction: Sugar-coated tablets are a popular solid dosage form in the pharmaceutical industry, offering advantages such as ease of swallowing, masking of unpleasant tastes, and aesthetic appeal. However, achieving a consistent and uniform color distribution during the sugar-coating process can be…

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Solid Dosage form, Tablets

Addressing Overheating Issues in HVAC Systems for High-Volume Tablet Production

Posted on March 17, 2025 By Admin

Addressing Overheating Issues in HVAC Systems for High-Volume Tablet Production Addressing Overheating Issues in HVAC Systems for High-Volume Tablet Production Introduction: In the pharmaceutical industry, maintaining optimal environmental conditions is crucial for the manufacturing of solid dosage forms, particularly tablets. HVAC (Heating, Ventilation, and Air Conditioning) systems play a vital role in regulating temperature and…

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Solid Dosage form, Tablets

Managing Material Shrinkage in Heat-Sealed Tablet Pouches

Posted on March 16, 2025 By Admin

Managing Material Shrinkage in Heat-Sealed Tablet Pouches Managing Material Shrinkage in Heat-Sealed Tablet Pouches Introduction: In the pharmaceutical industry, the packaging of solid dosage forms such as tablets is crucial for maintaining their integrity, efficacy, and shelf life. Heat-sealed tablet pouches are a popular choice due to their protective properties and ease of use. However,…

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Solid Dosage form, Tablets

Posts pagination

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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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