Whitepaper: Regulatory Landscape for Transition to Low Global Warming Potential (LGWP) Propellants for Pressurised Metered Dose Inhalers (pMDIs)
Published Dec 06, 2024
Published 02nd October 2023
In the domain of Pharmaceutical Regulatory Affairs, regulatory agencies such as EMA and FDA are harnessing the potential of Artifical Intelligence (AI) to revolutionise assessment and oversight. While EMA and FDA are in consultation with stakeholders, we explore AI’s transformative impact and potential challenges ahead. AI enables machines to learn, think, and perform human like tasks, particularly excelling in data analysis and decision making.
Published Dec 06, 2024
Published Dec 03, 2024
Published Dec 02, 2024
Published Nov 28, 2024
Published Nov 15, 2024
Published Nov 12, 2024
Published Oct 21, 2024
Published Oct 10, 2024
Published Oct 07, 2024