Skip to content

Pharma.Tips

Unlocking Pharma's Secrets: Your Ultimate Guide to Pharmaceutical Success!

Tag: Pharmaceutical manufacturing

Troubleshooting Residual Detergent Issues in Cleaning Validation for Rotary Coating Pans

Posted on May 9, 2025 By Admin

Troubleshooting Residual Detergent Issues in Cleaning Validation for Rotary Coating Pans Troubleshooting Residual Detergent Issues in Cleaning Validation for Rotary Coating Pans Introduction: In the pharmaceutical industry, ensuring the cleanliness of manufacturing equipment is paramount to maintaining product quality and patient safety. Rotary coating pans, essential in the production of coated tablets, must be meticulously…

Read More “Troubleshooting Residual Detergent Issues in Cleaning Validation for Rotary Coating Pans” »

Solid Dosage form, Tablets

Ensuring Moisture Protection in Primary Packaging for Enteric-Coated Tablets

Posted on May 8, 2025 By Admin

Ensuring Moisture Protection in Primary Packaging for Enteric-Coated Tablets Ensuring Moisture Protection in Primary Packaging for Enteric-Coated Tablets Introduction: In the pharmaceutical industry, ensuring the stability and efficacy of enteric-coated tablets is critical. These tablets are specifically designed to pass through the stomach intact and dissolve in the intestine. Moisture exposure can compromise the integrity…

Read More “Ensuring Moisture Protection in Primary Packaging for Enteric-Coated Tablets” »

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…

Read More “Managing Documentation Deviations in Process Validation Protocols” »

Solid Dosage form, Tablets

Managing Over-Spray in Sugar-Coating Processes During Validation Runs

Posted on May 6, 2025 By Admin

Managing Over-Spray in Sugar-Coating Processes During Validation Runs Managing Over-Spray in Sugar-Coating Processes During Validation Runs Introduction: In the pharmaceutical industry, sugar-coating is a critical process for tablet production. It enhances the aesthetic appeal, masks unpleasant tastes, and provides a protective layer to the active pharmaceutical ingredients (APIs). However, managing over-spray during sugar-coating can present…

Read More “Managing Over-Spray in Sugar-Coating Processes During Validation Runs” »

Solid Dosage form, Tablets

Troubleshooting Failures in Layer Adhesion During Bilayer Tablet Equipment Validation

Posted on May 6, 2025 By Admin

Troubleshooting Failures in Layer Adhesion During Bilayer Tablet Equipment Validation Troubleshooting Failures in Layer Adhesion During Bilayer Tablet Equipment Validation Introduction: Bilayer tablets have emerged as a significant advancement in pharmaceutical dosage forms, offering the potential for controlled release, improved patient compliance, and enhanced therapeutic efficacy. However, their manufacturing presents unique challenges, particularly concerning layer…

Read More “Troubleshooting Failures in Layer Adhesion During Bilayer Tablet Equipment Validation” »

Solid Dosage form, Tablets

Addressing Cross-Contamination Risks in Shared Tablet Manufacturing Equipment

Posted on May 5, 2025 By Admin

Addressing Cross-Contamination Risks in Shared Tablet Manufacturing Equipment Addressing Cross-Contamination Risks in Shared Tablet Manufacturing Equipment Introduction: In the pharmaceutical industry, ensuring the safety and efficacy of drug products is paramount. With the increasing demand for diverse medications, many manufacturers utilize shared equipment for tablet production to optimize resources. However, shared equipment can pose significant…

Read More “Addressing Cross-Contamination Risks in Shared Tablet Manufacturing Equipment” »

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…

Read More “Ensuring Robustness in QA Monitoring for Immediate Release Tablets” »

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…

Read More “Managing Adhesion Failures in Sustained Release Tablet Coating Layers During Validation” »

Solid Dosage form, Tablets

Ensuring Consistency in Granule Size Distribution During Validation Testing

Posted on May 4, 2025 By Admin

Ensuring Consistency in Granule Size Distribution During Validation Testing Ensuring Consistency in Granule Size Distribution During Validation Testing Introduction: In the pharmaceutical industry, ensuring consistency in granule size distribution during validation testing is crucial for the production of high-quality solid dosage forms, particularly tablets. Granule size directly influences the flowability, compressibility, and dissolution rates of…

Read More “Ensuring Consistency in Granule Size Distribution During Validation Testing” »

Solid Dosage form, Tablets

Troubleshooting Non-Uniform Layer Adhesion in Coating Machines During Validation

Posted on May 4, 2025 By Admin

Troubleshooting Non-Uniform Layer Adhesion in Coating Machines During Validation Troubleshooting Non-Uniform Layer Adhesion in Coating Machines During Validation Introduction: In the world of pharmaceutical manufacturing, the coating of tablets is a critical step that ensures the delivery of active pharmaceutical ingredients (APIs) with precision and efficacy. A uniform coating not only enhances the aesthetic appeal…

Read More “Troubleshooting Non-Uniform Layer Adhesion in Coating Machines During Validation” »

Solid Dosage form, Tablets

Validating Cleaning Effectiveness for Wet Granulation Equipment

Posted on May 4, 2025 By Admin

Validating Cleaning Effectiveness for Wet Granulation Equipment Validating Cleaning Effectiveness for Wet Granulation Equipment Introduction: In the pharmaceutical industry, maintaining the cleanliness and functionality of equipment is paramount to ensuring product quality and patient safety. Wet granulation, a critical step in tablet production, involves the agglomeration of powder particles using a liquid binder. This process,…

Read More “Validating Cleaning Effectiveness for Wet Granulation Equipment” »

Solid Dosage form, Tablets

Managing Surface Erosion in Sugar-Coated Tablets During Stability Studies

Posted on May 3, 2025 By Admin

Managing Surface Erosion in Sugar-Coated Tablets During Stability Studies Managing Surface Erosion in Sugar-Coated Tablets During Stability Studies Introduction: In the pharmaceutical industry, sugar-coated tablets have been a popular choice for delivering active pharmaceutical ingredients (APIs) due to their aesthetic appeal, ease of swallowing, and ability to mask the taste of certain drugs. However, during…

Read More “Managing Surface Erosion in Sugar-Coated Tablets During Stability Studies” »

Solid Dosage form, Tablets

Posts pagination

Previous 1 … 6 7 8 … 65 Next
  • 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

Copyright © 2025 Pharma.Tips.

Powered by PressBook WordPress theme