Tag: Validation Standards

Validating Rinse Volume Requirements in Cleaning Validation Protocols

May 15, 2025 Admin

Validating Rinse Volume Requirements in Cleaning Validation Protocols Validating Rinse Volume Requirements in Cleaning Validation Protocols Introduction: In the pharmaceutical industry, ensuring that manufacturing equipment is free from contaminants is paramount to product safety and efficacy. Cleaning validation is a critical component of Good Manufacturing Practice (GMP) to confirm that cleaning processes are effective and…

Solid Dosage form, Tablets

Poor validation of analytical methods for capsule testing.

April 18, 2025 Admin

Poor validation of analytical methods for capsule testing. Poor validation of analytical methods for capsule testing. Introduction: The validation of analytical methods is a critical component of pharmaceutical development and manufacturing, especially for solid oral dosage forms like capsules. Both hard and soft gelatin capsules require precise and reliable analytical methods to ensure their safety,…

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

Troubleshooting Non-Adherence to Cleanroom Validation Standards for Particle Monitoring

March 2, 2025 Admin

Troubleshooting Non-Adherence to Cleanroom Validation Standards for Particle Monitoring Troubleshooting Non-Adherence to Cleanroom Validation Standards for Particle Monitoring Introduction: In the pharmaceutical industry, maintaining a pristine environment is paramount to ensuring product quality and patient safety. Cleanrooms play a crucial role in this process, particularly in the manufacturing of solid dosage forms like tablets. A…

Solid Dosage form, Tablets