In this episode of the SNMMI Value Initiative Podcast, PharmaLogic’s Taylor Prejna speaks with Jessica Comstock, Vice President of Quality Assurance and Regulatory Affairs, about why quality and regulatory expertise is essential to successful radiopharmaceutical development. They explore the unique demands of the modality, from short product timelines and evolving regulations to isotope supply and global commercialization, and discuss how early collaboration with a CDMO’s quality and regulatory teams can reduce risk, support scalability, and ultimately improve patient access.
This podcast is sponsored by PharmaLogic, a Value Initiative member.
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