by Dr. Yashashwini Reddy | May 6, 2025
The Instrument and Equipment List for Pharmaceuticals refers to the various tools, devices, and machinery used in the pharmaceutical industry to conduct research, development, production, and quality control. These instruments ensure the safe, efficient, and compliant...
by Dr. Yashashwini Reddy | May 6, 2025
Qualified Persons (QPs) play a critical role in the pharmaceutical industry by overseeing the safety, efficacy, and compliance of medicines. They are responsible for ensuring that pharmaceutical products meet stringent regulatory standards and are safe for public use....
by Dr. Yashashwini Reddy | May 6, 2025
A Checklist to Review Tablet Process Validation is essential for ensuring that tablet manufacturing processes are consistently producing products that meet predefined specifications and regulatory requirements. Process validation in pharmaceutical manufacturing is a...
by Dr. Yashashwini Reddy | May 6, 2025
Here’s a detailed checklist for auditing an ointment manufacturing facility, aligned with Good Manufacturing Practices (GMP), regulatory expectations (such as USFDA, WHO, EU-GMP), and quality standards. The checklist is categorized for clarity: 1. General...
by Dr. Yashashwini Reddy | May 6, 2025
Handling and Control of Spills in Pharmaceutical Manufacturing Environments 1. Introduction Spillage in pharmaceutical manufacturing can lead to contamination, safety hazards, equipment damage, and regulatory non-compliance. Proper handling and control of spills is...
