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Tune in to Episode 2 of ACRO's Good Clinical Podcast, where Stephen Pyke and the FDA's Dr. Tala Fakhouri discuss the massive potential of AI in clinical research. 🎙   Learn more about the FDA's evidentiary standards for AI, the importance of methodological transparency in submissions and how AI stands to streamline the drug development process, helping to bring life-changing medicines to market more efficiently. 💡 Stephen also sheds light on where AI advancements will show up and what it means for patients. 👇 Watch below! Don’t miss this fascinating discussion. Access the full episode here: https://lnkd.in/gdMz_agR #ACRO #GoodClinicalPodcast #ArtificialIntelligence 

Jonathan Shough

Chief Information Officer, Parexel

1mo

He’s read all those books too! Thank you for your leadership on this topic with ACRO and within our clinical operations at Parexel.

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Thank you for your leadership, Stephen Pyke!

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Nitesh Kumar

Drug Safety Associate - 1 Regulatory affairs specialist, Veeva Vault -RIM,Global Regulatory affairs operation,Data Governance SPOR, xEVMPD,IDMP, UAT, Medical devices -Data operations-USFDA, EU.

1mo

Great advice!

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