Skip to content

Pharma.Tips

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

Tag: solid dosage forms

Addressing Cross-Contamination Risks in Blending Equipment During Cleaning Validation

Posted on May 19, 2025 By Admin

Addressing Cross-Contamination Risks in Blending Equipment During Cleaning Validation Addressing Cross-Contamination Risks in Blending Equipment During Cleaning Validation Introduction: The pharmaceutical industry is committed to ensuring the safety and efficacy of its products. One critical component of this commitment is the prevention of cross-contamination, particularly in the manufacturing of solid dosage forms like tablets. Blending…

Read More “Addressing Cross-Contamination Risks in Blending Equipment During Cleaning Validation” »

Solid Dosage form, Tablets

Troubleshooting Non-Adherence to Visual Inspection Standards During Equipment Validation

Posted on May 18, 2025 By Admin

Troubleshooting Non-Adherence to Visual Inspection Standards During Equipment Validation Troubleshooting Non-Adherence to Visual Inspection Standards During Equipment Validation Introduction: In the pharmaceutical manufacturing industry, particularly in the production of solid dosage forms like tablets, maintaining rigorous quality control is paramount. One of the key components of quality assurance is adhering to visual inspection standards during…

Read More “Troubleshooting Non-Adherence to Visual Inspection Standards During Equipment Validation” »

Solid Dosage form, Tablets

Ensuring Adequate Process Controls for Hygroscopic Tablet Production

Posted on May 14, 2025 By Admin

Ensuring Adequate Process Controls for Hygroscopic Tablet Production Ensuring Adequate Process Controls for Hygroscopic Tablet Production Introduction: Hygroscopic tablets, known for their ability to absorb moisture from the environment, pose unique challenges in pharmaceutical manufacturing. Ensuring adequate process controls during their production is crucial for maintaining product stability, efficacy, and quality. This comprehensive guide delves…

Read More “Ensuring Adequate Process Controls for Hygroscopic Tablet Production” »

Solid Dosage form, Tablets

Ensuring Consistency in Layer Adhesion for Multi-Layer Tablets During Validation

Posted on May 10, 2025 By Admin

Ensuring Consistency in Layer Adhesion for Multi-Layer Tablets During Validation Ensuring Consistency in Layer Adhesion for Multi-Layer Tablets During Validation Introduction: In the pharmaceutical industry, multi-layer tablets are gaining prominence due to their ability to deliver multiple drugs or release profiles within a single dosage form. This complexity brings forth challenges, particularly in ensuring consistency…

Read More “Ensuring Consistency in Layer Adhesion for Multi-Layer Tablets During Validation” »

Solid Dosage form, Tablets

Optimizing Desiccant Placement for Sustained Release Tablet Packaging

Posted on May 9, 2025 By Admin

Optimizing Desiccant Placement for Sustained Release Tablet Packaging Optimizing Desiccant Placement for Sustained Release Tablet Packaging Introduction: In the pharmaceutical industry, the integrity of drug products is paramount, particularly for sustained release tablets that require precise control over their release mechanisms. A crucial aspect of ensuring the efficacy and safety of these medications is effective…

Read More “Optimizing Desiccant Placement for Sustained Release Tablet Packaging” »

Solid Dosage form, Tablets

Troubleshooting API Loss in Extended Release Tablets Stored at High Humidity

Posted on May 6, 2025 By Admin

Troubleshooting API Loss in Extended Release Tablets Stored at High Humidity Troubleshooting API Loss in Extended Release Tablets Stored at High Humidity Introduction: Extended release tablets are a cornerstone of modern pharmaceutical formulations, offering controlled release of active pharmaceutical ingredients (APIs) over time to improve patient compliance and therapeutic efficacy. However, when these tablets are…

Read More “Troubleshooting API Loss in Extended Release Tablets Stored at High Humidity” »

Solid Dosage form, Tablets

Ensuring Packaging Compatibility for Tablets with Extended Stability Requirements

Posted on May 4, 2025 By Admin

Ensuring Packaging Compatibility for Tablets with Extended Stability Requirements Ensuring Packaging Compatibility for Tablets with Extended Stability Requirements Introduction: In the pharmaceutical industry, ensuring the stability and efficacy of tablets throughout their shelf life is paramount. This is particularly critical for tablets with extended stability requirements. The compatibility between the packaging and the tablet formulation…

Read More “Ensuring Packaging Compatibility for Tablets with Extended Stability Requirements” »

Solid Dosage form, Tablets

Challenges in achieving uniform capsule transparency during validation.

Posted on May 3, 2025 By Admin

Challenges in achieving uniform capsule transparency during validation. Challenges in achieving uniform capsule transparency during validation. Introduction: In the pharmaceutical industry, the demand for consistent and high-quality solid oral dosage forms has never been greater. Among these, capsules, particularly hard and soft gelatin capsules, stand out due to their versatility and consumer preference for ease…

Read More “Challenges in achieving uniform capsule transparency during validation.” »

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

Addressing Seal Creasing in Strip Packaging Machines

Posted on April 26, 2025 By Admin

Addressing Seal Creasing in Strip Packaging Machines Addressing Seal Creasing in Strip Packaging Machines Introduction: In the world of pharmaceutical manufacturing, ensuring the integrity of packaging is crucial to maintain product efficacy and consumer safety. One common issue that manufacturers face is seal creasing in strip packaging machines. This not only affects the aesthetic appeal…

Read More “Addressing Seal Creasing in Strip Packaging Machines” »

Solid Dosage form, Tablets

Addressing Over-Drying Issues in Granulation During Validation Runs

Posted on April 24, 2025 By Admin

Addressing Over-Drying Issues in Granulation During Validation Runs Addressing Over-Drying Issues in Granulation During Validation Runs Introduction: In the pharmaceutical industry, granulation is a critical step in the production of solid dosage forms such as tablets. It involves the agglomeration of powder particles to form granules, which enhance the flowability and compressibility of the powder,…

Read More “Addressing Over-Drying Issues in Granulation During Validation Runs” »

Solid Dosage form, Tablets

Problems with ensuring proper cleaning of high-shear mixers used in formulation.

Posted on April 19, 2025 By Admin

Problems with ensuring proper cleaning of high-shear mixers used in formulation. Problems with ensuring proper cleaning of high-shear mixers used in formulation. Introduction: In the pharmaceutical industry, maintaining the cleanliness of high-shear mixers is vital for ensuring product quality and patient safety. These mixers are essential in the formulation of solid oral dosage forms, particularly…

Read More “Problems with ensuring proper cleaning of high-shear mixers used in formulation.” »

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

Ensuring Adequacy of Binder Distribution in Sustained Release Tablet Validation

Posted on April 19, 2025 By Admin

Ensuring Adequacy of Binder Distribution in Sustained Release Tablet Validation Ensuring Adequacy of Binder Distribution in Sustained Release Tablet Validation Introduction: In the complex world of pharmaceutical manufacturing, sustained release tablets represent a crucial advancement in medication delivery systems. These tablets offer numerous benefits, including improved patient compliance and enhanced bioavailability. However, the validation of…

Read More “Ensuring Adequacy of Binder Distribution in Sustained Release Tablet Validation” »

Solid Dosage form, Tablets

Posts pagination

Previous 1 2 3 … 11 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