by Dr. Yashashwini Reddy | Sep 2, 2025
📘 How to Write a Factory Acceptance Test (FAT) Protocol A Factory Acceptance Test (FAT) is a documented process conducted at the vendor’s premises to verify that equipment, systems, or instruments meet the agreed design, functional, and regulatory requirements before...
by Dr. Yashashwini Reddy | Sep 2, 2025
🔹 Various Types of Blenders and Their Purpose 1. Double Cone Blender (DCB) Purpose: Used for homogeneous mixing of dry powders and granules. Advantages: Gentle mixing, suitable for fragile materials, low shear force. Applications: Commonly used in powder mixing for...
by Dr. Yashashwini Reddy | Sep 1, 2025
⚙️ Equipment Lubricants in Pharmaceuticals In pharmaceutical manufacturing, lubricants are essential for smooth operation of equipment like tablet compression machines, granulators, blenders, filling lines, and packaging machinery. However, because of the high...
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...
