Pharmaceutical manufacturing requires defining quality target product profiles and critical quality attributes (CQAs) to ensure desired product quality. Process development identifies critical process ...

Continuous manufacturing and a quality-by-design development approach are a natural fit. FDA, as well as other regulatory agencies around the world, have for many years been encouraging drug makers to ...

QC laboratories perform a critical role in demonstrating pharmaceutical products are consistently manufactured, safe, potent, and pure. At the same time, the number of tests run by QC laboratories is ...

The pharmaceutical industry depends on quality and reliability, especially within the manufacturing and application of pharmaceutically active substances or excipients. There are two core objectives ...

Bioprocessing is an umbrella term that describes the research, development, manufacturing, and commercialization of products derived from or used by biological systems. For industrial purposes, ...

The process control and instrumentation minor emphasizes developing skills and knowledge in theory, software and in the field. Students graduate ready to solve complex control problems in the chemical ...

In the pharmaceutical and life sciences industries, the terms Quality Assurance (QA) and Quality Control (QC) are often used interchangeably, but they represent two distinct and critical functions ...

Currently, bioprocess monitoring and control systems rely on infrequent and time-consuming offline sampling methods. This can lead to loopholes in data and major gaps in knowledge, as well as ...

Recently published study by Prophecy Market Insights Pharmaceutical Microbiology Quality Control Market Size, Share & Trends Outlook Report [2025-2035] contains a detailed examination of major trends, ...

The pharmaceutical isolator market offers strategic growth via advanced contamination control technologies addressing sterility and compliance pressures. Key opportunities include scalable and ...