by Dr. Yashashwini Reddy | May 22, 2024
Drug Product Recall Procedure as per CDSCO Introduction In the pharmaceutical industry, ensuring the safety and quality of products is paramount. When defects or issues arise, a structured systemic recall procedure is essential to protect consumers and maintain...
by Dr. Yashashwini Reddy | May 20, 2024
Pharmaceutical products are recalled when there is a need to address issues related to quality, safety, and efficacy and recall is not a smaller term, in this article, we are going to learn about why products are recalled i.e. what are the product-related issues, and...
by Dr. Yashashwini Reddy | May 18, 2024
Environmental monitoring in a pharmaceutical manufacturing facility 1.0 Purpose This procedure defines the requirements for conducting viable and non-viable environmental monitoring in classified areas of the pharmaceutical manufacturing facility. Environmental...
by Dr. Yashashwini Reddy | May 15, 2024
In-process checks during compression by QA The IPQA person is responsible for performing the in-process checks at a predetermined frequency along with the production personnel to ensure quality products are consistently produced. As you know pharmaceutical products...
by Dr. Yashashwini Reddy | May 6, 2024
If you are attending a regulatory affairs interview, you cannot miss these interview questions in your preparation list, before attending the interview checking the previously asked questions is very crucial, because the interviewer is going to test your knowledge in...
