Tag: Pharma industry standards

Managing Cross-Contamination Risks in Coating Machines Used for Extended Release Tablets

May 23, 2025 Admin

Managing Cross-Contamination Risks in Coating Machines Used for Extended Release Tablets Managing Cross-Contamination Risks in Coating Machines Used for Extended Release Tablets Introduction: In the pharmaceutical industry, ensuring product safety and efficacy is paramount, and one critical aspect of this is managing cross-contamination risks. This is especially crucial in the production of extended-release tablets, where…

Solid Dosage form, Tablets

Difficulty in implementing real-time data monitoring systems for quality checks.

April 15, 2025 Admin

Difficulty in implementing real-time data monitoring systems for quality checks. Difficulty in implementing real-time data monitoring systems for quality checks. Introduction: In the rapidly advancing pharmaceutical industry, quality assurance remains a cornerstone of successful manufacturing processes, particularly for solid oral dosage forms like capsules. As the demand for higher quality and more consistent pharmaceutical products…

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

Problems with validating sterilization processes for gelatin solutions.

April 7, 2025 Admin

Problems with validating sterilization processes for gelatin solutions. Problems with validating sterilization processes for gelatin solutions. Introduction: Sterilization is a critical process in the pharmaceutical industry, especially for solid oral dosage forms like capsules. Gelatin solutions, used in both hard and soft gelatin capsules, require meticulous sterilization to ensure product safety and efficacy. However, validating…

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

Inadequate systems for reviewing and updating quality-related documents.

April 5, 2025 Admin

Inadequate systems for reviewing and updating quality-related documents. Inadequate Systems for Reviewing and Updating Quality-Related Documents Introduction: In the pharmaceutical industry, maintaining up-to-date and accurate quality-related documents is crucial. These documents ensure compliance with regulatory standards, facilitate efficient operations, and uphold product quality and safety. Despite their significance, many organizations struggle with inadequate systems for…

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

Addressing Challenges in Aluminum Blister Sealing for Extended Release Tablets

April 2, 2025 Admin

Addressing Challenges in Aluminum Blister Sealing for Extended Release Tablets Addressing Challenges in Aluminum Blister Sealing for Extended Release Tablets Introduction: In the pharmaceutical industry, the packaging of extended release tablets is crucial not only for maintaining the efficacy and safety of the product but also for ensuring patient compliance. Aluminum blister packs are commonly…

Solid Dosage form, Tablets

Inadequate systems for verifying capsule coating equipment calibration.

March 30, 2025 Admin

Inadequate systems for verifying capsule coating equipment calibration. Inadequate systems for verifying capsule coating equipment calibration. Introduction: In the pharmaceutical industry, the precision of capsule coating processes is critical for ensuring product quality and compliance with regulatory standards. Capsules, whether hard or soft gelatin, require exact coating specifications to achieve the desired therapeutic effect, stability,…

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

Troubleshooting Cleaning Validation Failures in Compression Machines for Multi-API Tablets

March 18, 2025 Admin

Troubleshooting Cleaning Validation Failures in Compression Machines for Multi-API Tablets Troubleshooting Cleaning Validation Failures in Compression Machines for Multi-API Tablets Introduction: In the pharmaceutical industry, ensuring the cleanliness of equipment is paramount, especially when manufacturing multi-active pharmaceutical ingredient (API) tablets. Cleaning validation is a critical process that confirms the effectiveness of cleaning procedures to prevent…

Solid Dosage form, Tablets

Managing Documentation Errors in Coating Processes

March 14, 2025 Admin

Managing Documentation Errors in Coating Processes Managing Documentation Errors in Coating Processes Introduction: In the pharmaceutical industry, coating processes are critical in ensuring that tablets meet both aesthetic and functional requirements. Proper documentation in these processes is vital, not only for maintaining quality and consistency but also for complying with regulatory standards. This article delves…

Solid Dosage form, Tablets

Validating Water Circulation Systems for Extended Release Tablet Equipment

March 7, 2025 Admin

Validating Water Circulation Systems for Extended Release Tablet Equipment Validating Water Circulation Systems for Extended Release Tablet Equipment Introduction: In the pharmaceutical industry, ensuring the quality and safety of extended release tablets is paramount. A critical aspect of this process is the validation of water circulation systems used in tablet manufacturing equipment. Water is a…

Solid Dosage form, Tablets

Identifying Failures in Adhesion Tests for Film Coatings

March 3, 2025 Admin

Identifying Failures in Adhesion Tests for Film Coatings Identifying Failures in Adhesion Tests for Film Coatings Introduction: In the pharmaceutical industry, film coatings on tablets serve multiple critical functions, including masking unpleasant tastes, enhancing tablet stability, and controlling drug release. Ensuring the adhesion of these coatings is vital for maintaining product integrity and efficacy. Failures…

Solid Dosage form, Tablets