by Dr. Yashashwini Reddy | Sep 1, 2025
🧪 Qualification Procedure for Vial Washing Machine A Vial Washing Machine is a critical equipment in sterile manufacturing, ensuring removal of particulate and microbial contamination before sterilization and filling. Its qualification ensures consistent performance...
by Dr. Yashashwini Reddy | Sep 1, 2025
🌬️ Basics of HVAC System in Pharmaceuticals 📌 What is HVAC? HVAC = Heating, Ventilation, and Air Conditioning.In pharmaceuticals, HVAC systems are critical to: Maintain controlled environment for manufacturing. Ensure product quality, safety, and regulatory...
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
📌 Effective Deviation Management in Pharmaceutical Manufacturing 🔹 What is a Deviation? A Deviation is any departure from approved processes, procedures, specifications, or GMP requirements that may impact product quality, safety, data integrity, or regulatory...
by Dr. Yashashwini Reddy | Aug 30, 2025
Standard Operating Procedure (SOP) for Cleaning of Depyrogenation Oven 1.0 Purpose To establish a procedure for the cleaning of the hot air depyrogenation oven used for removal of pyrogens from glassware and equipment, ensuring compliance with cGMP requirements and...
