Autonomy is not a binary option, Bryant said in the first part of this video interview with PharmTech ®, and can work in ...
The field of cancer treatment saw a variety of advancements in 2025, from new dedicated centers to approved treatments to ...
Digital GMP expectations are increasing, driven by Annex 11 and Annex 22, necessitating robust lifecycle management, data ...
In an expansion of his written three-part series for PharmTech, Jason Bryant of ArisGlobal explains the interplay between ...
The top 10 PharmTech videos of the year cover advanced therapies, high-concentration biologics, major mergers and ...
The year 2025 was defined by escalating global trade tensions that fundamentally reshaped the pharmaceutical supply chain, ...
In this overview, PharmTech takes a look back at significant news in the development and approval of cancer treatment in 2025.
FDA has taken steps to embrace AI in 2025, announcing in December that it will be providing agency staff with agentic AI ...
From a global regulatory perspective, Cytokinetics is expanding its footprint rapidly. The drug received approval in China on ...
Mike Stenberg, LGM Pharma, outlines how GLP-1s, AI, and 505(b)(2) delivery shifts are driving pharmaceutical innovation.
The revised EU pharmaceutical policy maintains eight-year data protection but reduces market protection to one year, ...
Multiple departments, including engineering and quality assurance, are responsible for evaluating GMP equipment and ...