Process development is the exercise of creating new and improved manufacturing methods, optimizing them in terms of time and financial efficiency while maintaining regulatory compliance and product ...

Pharmaceutical engineering is a powerful career pathway for students who want to turn scientific knowledge into medicines ...

Pharmaceutical manufacturing is entering a digital era. From AI and digital twins to supercomputers and quantum computing, ...

This webinar highlights the operational, quality, and efficiency benefits of integrating real-time Process Raman spectroscopy into pharmaceutical manufacturing, specifically during Hot Melt Extrusion ...

However, the rapid rise of automation, fintech integration, and data-driven manufacturing is transforming pharma production ...

In 2002, the U.S. Food and Drug Administration (FDA) launched the Pharmaceutical Quality for the 21st Century Initiative to encourage adoption of innovative technologies that would lead to an agile, ...

Containment is defined as the isolation of substances from the operator, from the environment and from other substances. Containment systems have to manage emissions and exposure, both generated by ...

Sustainable and environmentally friendly production processes are playing an increasingly important role in almost all branches of industry. The production of active pharmaceutical ingredients in ...

The compliance process at pharmaceutical manufacturers is complicated because many still use paper-based systems to record manufacturing steps. These paper records are reviewed by FDA auditors to ...

Environmental contamination control is a crucial aspect of sterile pharmaceutical manufacturing, and risk management is needed to guarantee that the necessary control procedures are in place. The risk ...

A pharmaceutical quality crisis involving nitrosamine contamination began in 2018 with the discovery of ...