by Dr. Yashashwini Reddy | May 2, 2025
The tablet manufacturing process is a complex and highly regulated series of steps that ensures the final product is safe, effective, and of consistent quality. Below is a detailed explanation of the key stages involved in tablet manufacturing: 1. Pre-Formulation...
by Dr. Yashashwini Reddy | May 2, 2025
Preparation of Master Formula Record (MFR) in Pharmaceutical Manufacturing The Master Formula Record (MFR) is a critical document in pharmaceutical manufacturing. It serves as a detailed guide for producing a specific batch of a pharmaceutical product, ensuring that...
by Dr. Yashashwini Reddy | Nov 29, 2024
Aseptic and Sterile Conditions in Pharma: Key Differences In the pharmaceutical industry, maintaining the highest standards of safety, quality, and efficacy is critical. Two key concepts in this context are aseptic conditions and sterile conditions. Though often used...
by Dr. Yashashwini Reddy | Nov 24, 2024
Common Blister Defects in Pharmaceutical Packaging: Identification and Solutions Blister packaging is a popular choice in the pharmaceutical industry due to its ability to safeguard products, enhance usability, and ensure tamper-proofing. However, defects during...
by Dr. Yashashwini Reddy | Nov 24, 2024
In Process-quality assurance personnel is responsible for giving the line clearance during the beginning of the manufacturing process. Line clearance activity looks easy, but it’s a task that must be executed with care as several checkpoints must be gone...
