by Dr. Yashashwini Reddy | Oct 24, 2024
In the pharmaceutical industry, Air Handling Units (AHUs) are critical for maintaining controlled environments in cleanrooms and production areas. They ensure that air quality standards are met, which is essential to prevent contamination during the production of...
by Dr. Yashashwini Reddy | Oct 22, 2024
Good Automated Manufacturing Practices (GAMP): Ensuring Quality in Pharma Automation In today’s fast-paced pharmaceutical industry, automation has become a key driver for improving efficiency, consistency, and maintaining the highest quality standards. To ensure...
by Dr. Yashashwini Reddy | Oct 8, 2024
“Key Responsibilities of the Qualification Department in Pharma” The qualification department plays a key role in the pharmaceutical industry by ensuring that all equipment, processes, and systems are thoroughly tested and validated to meet regulatory and...
by Dr. Yashashwini Reddy | Sep 9, 2024
GMP vs. cGMP in Pharma: What’s the Difference? In the pharmaceutical world, making safe and high-quality medicines is essential. That’s where GMP (Good Manufacturing Practices) and cGMP (Current Good Manufacturing Practices) come in. While they sound similar, they...
by Dr. Yashashwini Reddy | May 16, 2024
A Site Acceptance Test (SAT) is performed to know whether the system meets the required specifications and complies with the needs of the user. This on-site test is written, and executed by the client and involves thorough inspections and testing of system...
