I am honored to have participated in Pharma's Almanac's recent roundtable, where industry leaders discussed the pivotal regulatory decisions shaping the future of biopharma in 2024 and beyond. In my contribution, I highlighted the emerging regulatory framework for generative AI technologies. As we integrate these technologies into drug development and patient care, it is crucial to establish responsible usage guidelines that minimize bias in AI outputs. Read the full roundtable discussion to gain insights from industry experts on the dynamic regulatory landscape that will drive innovation and ensure safety across the sector. https://lnkd.in/g-yU58uV #Biopharma #AI #Innovation #Regulation
In case you missed it: in this Pharma's Almanac roundtable, a panel of industry experts weighs in on the most significant regulatory decision or guidance influencing biopharma in 2024 and beyond. Read the roundtable here: https://lnkd.in/g-yU58uV Our roundtable includes contributors from GBI Bio, Lonza, MilliporeSigma, PPD, Samsung Biologics, Tedor Pharma Services, ADVI Health, Agilent Technologies, Astrea Bioseparations, Atomic AI, BioBridge Global, BioIVT, BIOSENIC S.A., Bruker BioSpin, Cellares, Cyclacel Limited, eClinical Solutions, Ellab - Validation & Monitoring Solutions, Evonik, Faeth Therapeutics, HDT Bio, Likarda, LGM Pharma, Medicus Pharma Ltd., Mission Bio, MOBILion Systems, Inc., Newfront, Norstella, OM1, Inc., OrganaBio, Organon, Ori Biotech, OzUK, Pharmatech Associates, a USP company, PointClickCare, ScaleReady, SCIEX, SCTbio, Sernova, ...(cont) #Regulatory #Biopharma #Roundtable