Skip to content

Pharma.Tips

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

Tag: Pharmaceutical safety

Preventing Mislabeling in High-Speed Packaging Lines for Multi-Layer Tablets

Posted on March 17, 2025 By Admin

Preventing Mislabeling in High-Speed Packaging Lines for Multi-Layer Tablets Preventing Mislabeling in High-Speed Packaging Lines for Multi-Layer Tablets Introduction: In the fast-paced world of pharmaceutical manufacturing, the efficiency and accuracy of high-speed packaging lines are crucial for ensuring the safety and efficacy of multi-layer tablets. Mislabeling can lead to serious consequences, including patient safety risks,…

Read More “Preventing Mislabeling in High-Speed Packaging Lines for Multi-Layer Tablets” »

Solid Dosage form, Tablets

Managing Static Charge in Granule Transfer Systems

Posted on March 12, 2025 By Admin

Managing Static Charge in Granule Transfer Systems Managing Static Charge in Granule Transfer Systems Introduction: In the pharmaceutical industry, the efficient transfer of granules is crucial for the production of solid dosage forms like tablets. However, one of the persistent challenges faced during this process is the management of static charge. Static electricity can cause…

Read More “Managing Static Charge in Granule Transfer Systems” »

Solid Dosage form, Tablets

Optimizing Batch Coding Placement on Tablet Packaging Materials

Posted on March 8, 2025 By Admin

Optimizing Batch Coding Placement on Tablet Packaging Materials Optimizing Batch Coding Placement on Tablet Packaging Materials Introduction: The pharmaceutical industry is highly regulated, with stringent requirements for product safety, traceability, and compliance. One critical aspect of pharmaceutical packaging is the placement of batch coding on tablet packaging materials. Batch codes are essential for traceability, allowing…

Read More “Optimizing Batch Coding Placement on Tablet Packaging Materials” »

Solid Dosage form, Tablets

Troubleshooting Moisture Loss in Coated Tablets Stored at Low Humidity

Posted on March 7, 2025 By Admin

Troubleshooting Moisture Loss in Coated Tablets Stored at Low Humidity Troubleshooting Moisture Loss in Coated Tablets Stored at Low Humidity Introduction: In the pharmaceutical industry, maintaining the stability and efficacy of drug products is paramount. Coated tablets, a common solid dosage form, are often designed with specific moisture content to ensure their integrity and therapeutic…

Read More “Troubleshooting Moisture Loss in Coated Tablets Stored at Low Humidity” »

Solid Dosage form, Tablets

Managing Static Charge in Powder Handling Systems During Production

Posted on March 7, 2025 By Admin

Managing Static Charge in Powder Handling Systems During Production Managing Static Charge in Powder Handling Systems During Production Introduction: In the world of pharmaceutical manufacturing, maintaining the integrity and safety of production processes is paramount. One often overlooked but critical aspect is the management of static charge in powder handling systems. Static electricity can cause…

Read More “Managing Static Charge in Powder Handling Systems During Production” »

Solid Dosage form, Tablets

Addressing Cross-Contamination Risks in Purified Water Systems for Multi-API Tablets

Posted on March 5, 2025 By Admin

Addressing Cross-Contamination Risks in Purified Water Systems for Multi-API Tablets Addressing Cross-Contamination Risks in Purified Water Systems for Multi-API Tablets Introduction: In the pharmaceutical industry, the production of multi-Active Pharmaceutical Ingredient (API) tablets poses unique challenges, particularly concerning cross-contamination. Purified water systems play a pivotal role in tablet manufacturing, serving as a critical utility in…

Read More “Addressing Cross-Contamination Risks in Purified Water Systems for Multi-API Tablets” »

Solid Dosage form, Tablets

Validating Rinse Sampling Protocols for Cleaning Validation in Multi-Product Facilities

Posted on March 5, 2025 By Admin

Validating Rinse Sampling Protocols for Cleaning Validation in Multi-Product Facilities Validating Rinse Sampling Protocols for Cleaning Validation in Multi-Product Facilities Introduction: In the dynamic field of pharmaceutical manufacturing, maintaining stringent hygiene and safety standards is paramount. Multi-product facilities, which handle the production of various drugs using shared equipment, face unique challenges in preventing cross-contamination. A…

Read More “Validating Rinse Sampling Protocols for Cleaning Validation in Multi-Product Facilities” »

Solid Dosage form, Tablets

Managing Cross-Contamination Risks in Fluid Bed Granulators for Multi-Layer Tablets

Posted on March 4, 2025 By Admin

Managing Cross-Contamination Risks in Fluid Bed Granulators for Multi-Layer Tablets Managing Cross-Contamination Risks in Fluid Bed Granulators for Multi-Layer Tablets Introduction: In the pharmaceutical industry, the production of multi-layer tablets requires meticulous attention to detail to ensure product safety and efficacy. One critical aspect of tablet production is the use of fluid bed granulators, which…

Read More “Managing Cross-Contamination Risks in Fluid Bed Granulators for Multi-Layer Tablets” »

Solid Dosage form, Tablets

Addressing Cross-Contamination Risks in Shared Utility Lines for Coated Tablets

Posted on March 3, 2025 By Admin

Addressing Cross-Contamination Risks in Shared Utility Lines for Coated Tablets Addressing Cross-Contamination Risks in Shared Utility Lines for Coated Tablets Introduction: In the pharmaceutical industry, maintaining product integrity and patient safety is paramount. One of the significant challenges faced by manufacturers is the risk of cross-contamination, especially when utilizing shared utility lines for coated tablets….

Read More “Addressing Cross-Contamination Risks in Shared Utility Lines for Coated Tablets” »

Solid Dosage form, Tablets

Troubleshooting Failures in Residual Solvent Analysis for Utility Validation Studies

Posted on March 3, 2025 By Admin

Troubleshooting Failures in Residual Solvent Analysis for Utility Validation Studies Troubleshooting Failures in Residual Solvent Analysis for Utility Validation Studies Introduction: In the pharmaceutical industry, ensuring the safety and efficacy of products is paramount. Residual solvent analysis plays a critical role in utility validation studies, which are essential to maintaining the integrity of solid dosage…

Read More “Troubleshooting Failures in Residual Solvent Analysis for Utility Validation Studies” »

Solid Dosage form, Tablets

What are the advantages of using pre-formulated direct compression excipients?

Posted on August 22, 2023August 5, 2023 By Admin

Advantages of Using Pre-formulated Direct Compression Excipients Pre-formulated direct compression excipients are ready-to-use blends of various excipients specifically designed for direct compression tablet manufacturing. These pre-formulated excipients offer several advantages over traditional individual excipients. Here are the key advantages of using pre-formulated direct compression excipients: 1. Simplified Formulation Development Pre-formulated excipients streamline the tablet formulation…

Read More “What are the advantages of using pre-formulated direct compression excipients?” »

Tablets

How are multi-layer tablets manufactured?

Posted on August 22, 2023August 5, 2023 By Admin

Manufacturing Process of Multi-Layer Tablets Multi-layer tablets are pharmaceutical tablets that consist of two or more distinct layers of different drug formulations. These layers may release the active pharmaceutical ingredients (APIs) at different rates or provide other specific functionalities, such as immediate release followed by sustained release. The manufacturing process of multi-layer tablets involves careful…

Read More “How are multi-layer tablets manufactured?” »

Tablets

Posts pagination

Previous 1 2 3 … 8 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