by Dr. Yashashwini Reddy | Aug 30, 2025
Standard Operating Procedure (SOP) for Cleaning of Deep Freezer 1.0 Purpose To define the procedure for cleaning and maintaining the deep freezer to ensure proper functioning, prevent contamination, and maintain sample integrity. 2.0 Scope This SOP applies to all deep...
by Dr. Yashashwini Reddy | May 2, 2025
Equipment malfunction in pharmaceutical production can have wide-ranging and serious implications, affecting not only operational efficiency but also regulatory compliance, product quality, and patient safety. Here’s a detailed explanation of how such malfunctions can...
by Dr. Yashashwini Reddy | Apr 10, 2025
The need for regulatory affairs (RA) professionals is prominently recognized within the pharmaceutical sector, consulting firms, clinical research organizations, and regulatory bodies. As I contemplated my career shift from laboratory science to regulatory affairs, I...
by Dr. Yashashwini Reddy | Apr 8, 2025
Regulatory Affairs professionals are responsible for ensuring that products and processes adhere to applicable regulations and standards, thereby protecting public health and safety. They collaborate with regulatory agencies, prepare and submit necessary applications,...
by Dr. Yashashwini Reddy | Nov 27, 2024
Q1. What is disintegration, and why is it important in tablet evaluation? A: Disintegration is the process by which a tablet breaks down into smaller fragments in a liquid medium to release its active ingredients. It is important because proper disintegration is a...
