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...
by Dr. Yashashwini Reddy | May 8, 2024
Quality assurance interview questions in Pharma These are the most frequently asked interview questions in the Quality Assurance Department if you are a fresher looking for a job opportunity, in quality assurance then these are basic questions that are asked. Define...
