by Dr. Yashashwini Reddy | Aug 18, 2025
📘 Preparation of Master Formula Record (MFR) A Master Formula Record (MFR) is a controlled document that serves as a blueprint for manufacturing a pharmaceutical product. It ensures product quality, consistency, and compliance with regulatory requirements. 🔑 Key Steps...
by Dr. Yashashwini Reddy | Aug 12, 2025
Sampling and Testing in Exhibit and Process Validation Batches 1. Introduction Exhibit Batches: Produced at commercial scale (or pilot scale in some cases) before product launch, used to demonstrate manufacturing feasibility and generate stability, quality, and...
by Dr. Yashashwini Reddy | Aug 12, 2025
Quality Management System (QMS) 1. Definition A Quality Management System (QMS) is a structured framework of policies, procedures, processes, and resources that ensures pharmaceutical products consistently meet quality, safety, efficacy, and regulatory requirements.It...
by Dr. Yashashwini Reddy | Aug 11, 2025
Calibration of Automatic Potentiometric Titrator in Pharmaceuticals 1. Introduction An automatic potentiometric titrator is widely used in pharmaceutical laboratories for accurate and reproducible titrations, such as acid-base, redox, complexometric, and non-aqueous...
by Dr. Yashashwini Reddy | Aug 11, 2025
Calibration of Brookfield Viscometer in Pharmaceuticals 1. Introduction A Brookfield viscometer is widely used in pharmaceutical industries to measure the viscosity of semi-solids, creams, gels, and certain liquid formulations.Regular calibration ensures accuracy,...
