Continued process verification (CPV) is the third stage of the product lifecycle of any medicine either within the small or large molecule arena. The CPV is the subsequent step to process design ...

Researchers at the University of Liège (BE) have designed a high-performance, open-access continuous flow process to safely produce key antibacterial drugs from bio-based furfural. The results of the ...

DIANT is a startup co-founded by Antonio Costa, Ph.D. and Diane Burgess, Ph.D. In 2020, DIANT licensed their core manufacturing technology from UConn and was granted a patent on the technology earlier ...

In March 2023, the FDA issued a final guidance, titled “Q13 Continuous Manufacturing of Drug Substances and Drug Products” that describes scientific and regulatory considerations for the development, ...

Boost ROI through automation, AI, digital twins, modular single-use systems and partnerships that cut costs, improve quality, scale production and speed time to market.Dublin, Oct. 01, 2026 (GLOBE ...

Huang: Innovations such as integrated bioprocess and other technologies are key to increase productivity and shorten development timelines and to bring more candidates into clinical development. We ...

At the AAPS 2024 PharmSci 360 conference in Salt Lake City, Scott Krull, a chemical engineer at the FDA Office of Pharmaceutical Quality, provided a comprehensive overview of the regulatory framework ...

The pharmaceutical industry plays a central role in Singapore’s economy and is a key pillar of the country’s high-value manufacturing strategy. Eight of the world’s top 10 biopharmaceutical companies ...

Next generation continuous direct compression (CDC) platform, jointly developed with GEA, to bring a continuous tableting ...

While moving from batch to continuous manufacturing may not be new in many other industries, it is in pharmaceutical and biotech manufacturing. According to Laura Wareham, Senior Scientist, ...