by Dr. Yashashwini Reddy | Sep 2, 2025
Spillage Management in Pharmaceutical Production Area Spillages in pharmaceutical production areas can pose serious risks including contamination, product quality compromise, safety hazards, and regulatory non-compliance. Effective spillage management ensures product...
by Dr. Yashashwini Reddy | Sep 2, 2025
📌 Restricted Access Barrier System (RABS) in Pharmaceuticals A Restricted Access Barrier System (RABS) is an advanced containment and protection technology used in pharmaceutical sterile manufacturing to reduce contamination risks. It provides a physical and...
by Dr. Yashashwini Reddy | Sep 1, 2025
🌡️ Different Types of Temperature Sensors 1. Thermocouples Principle: Seebeck effect (voltage generated at junction of two dissimilar metals). Range: –200 °C to +1800 °C (depending on type: J, K, T, R, S). Pros: Wide range, rugged, fast response. Cons: Lower accuracy...
by Dr. Yashashwini Reddy | Aug 30, 2025
Standard Operating Procedure (SOP) for Operation of Water Bath 1.0 Purpose To define the procedure for the correct operation of the water bath to ensure uniform and controlled heating of laboratory samples. 2.0 Scope This SOP applies to all Quality Control (QC),...
by Dr. Yashashwini Reddy | Aug 29, 2025
1. Purpose To establish a procedure for environmental monitoring of the manufacturing area to ensure controlled conditions and compliance with cGMP requirements. 2. Scope This SOP applies to all classified manufacturing areas (Grade A, B, C, and D) where sterile or...
