by Dr. Yashashwini Reddy | Sep 2, 2025
🔹 Types of Stainless Steel in Pharmaceuticals 1. SS 304 / 304L (AISI 304) Composition: 18% Cr, 8% Ni 304L = low carbon version → better weldability, less sensitization Applications: Non-contact parts (frames, supports, furniture, piping for non-critical utilities)...
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
🧪 Validation of Clean Room Pass Boxes 📌 What is a Pass Box? A Pass Box is an enclosure fitted between two cleanroom areas or between a cleanroom and a non-cleanroom. It allows transfer of materials while minimizing cross-contamination and maintaining cleanroom...
by Dr. Yashashwini Reddy | Sep 1, 2025
🧼 Cleaning Validation of CIP Systems in Pharmaceuticals 🔹 What is CIP? Clean-in-Place (CIP) is an automated method for cleaning process equipment (bioreactors, fermenters, tanks, piping, filling lines) without disassembly. Ensures removal of residues (API, excipients,...
