Two weeks after launch, 91% of people had confirmed that they had completed the training. That level of visibility ...
USP is developing digital reference standards to integrate into modern digital environments, enhancing regulatory confidence ...
The cell and gene therapy sector has never lacked attention, but all too often, the narrative swings from one extreme to ...
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 ...
New York, New York--(Newsfile Corp. - January 7, 2026) - Frost & Sullivan has released a white paper titled, "How Leading Global Pharma Embraces AI to Automate Regulatory and Medical Documents with ...
The development and release of pharmaceutical products require the use of modern, efficient, and adaptable analytical techniques to assure efficacy and patient safety. The growing interest in complex ...
Advanced technologies in pharma manufacturing necessitate a redefinition of the Qualified Person's role, focusing on digital and data-driven environments. Continuous manufacturing and AI introduce new ...
Paris, France; Munich, Germany – May 18, 2020 – Atos, a global leader in digital transformation and Siemens, a global engineering leader, are working together with the pharmaceutical industry to ...
Selvaraja Elumalai - distinguished quality control professionals with an experience of more than twenty years in the pharmaceutical industry. He has a solid foundation in physical chemistry and is ...
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 ...
Bioprinting is rapidly moving from research labs into commercial reality, and it is reshaping how the pharmaceutical and biotechnology industries think about drug development, regenerative medicine, ...