by Dr. Yashashwini Reddy | Aug 12, 2025
CAPA Documentation: Common Mistakes to Avoid Definition:Corrective and Preventive Actions (CAPA) are processes used in pharmaceutical quality systems to investigate, address, and prevent the recurrence of deviations, non-conformances, or quality issues. Proper...
by Dr. Yashashwini Reddy | Aug 12, 2025
Change Control in Pharmaceuticals Definition:Change control is a formal GMP-compliant system used to manage and document any change in processes, equipment, materials, methods, documents, or facilities to ensure that product quality, safety, and regulatory...
by Dr. Yashashwini Reddy | Aug 11, 2025
Calibration of Halogen Moisture Analyzer in Pharmaceuticals 1. Introduction A Halogen Moisture Analyzer determines the moisture content of a sample by heating it with a halogen lamp and continuously measuring the weight loss until a constant mass is...
by Dr. Yashashwini Reddy | Aug 9, 2025
Limitations in Dissolution Testing Poor In-Vivo Correlation (IVIVC) Dissolution data may not accurately predict drug release in the human body due to complex gastrointestinal (GI) conditions. Single-Media Testing Conventional USP tests often use only one dissolution...
by Dr. Yashashwini Reddy | Aug 9, 2025
The Shape of Pharmaceutical Dosage Forms Definition:In pharmaceuticals, dosage form shape refers to the physical appearance and geometry of the medicine, which can influence patient compliance, swallowing ease, identification, and manufacturing efficiency. 1. Solid...
