by Dr. Yashashwini Reddy | Sep 2, 2025
How to calculate To calculate the capacity of tablet coating pan we need two factors which are given as below, Brimful volume of pan Tablet bulk density Bring full volume is the volume of the water which can be added in the tablet coating pan up to its brim or upper...
by Dr. Yashashwini Reddy | Sep 2, 2025
Generic Drugs Manufacturing: Opportunities and Obstacles Opportunities: Cost-effectiveness: Generic drugs offer patients affordable alternatives to branded medicines, increasing accessibility and market demand. Patent Expiry of Blockbuster Drugs: As patents of many...
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 1, 2025
📘 Preparation of Master Formula Record (MFR) 📌 What is MFR? A Master Formula Record (MFR) is a controlled document that provides the recipe, manufacturing process, equipment, materials, and in-process controls required to produce a pharmaceutical product. It is...
by Dr. Yashashwini Reddy | Aug 29, 2025
1. Purpose To establish a standard procedure for monitoring non-viable airborne particulate matter in controlled manufacturing areas to ensure compliance with ISO 14644, EU GMP Annex 1, and regulatory requirements for sterile manufacturing. 2. Scope This SOP applies...
