Establishing Release Criteria for Quality Control Testing of Irregular Chelators, Antibodies, Isotopes & Whole Drug Product
Time: 9:00 am
day: Workshop A
At this symposium, we emphasize the significance of proven quality in ensuring safety and maintaining high standards across the radiopharmaceutical landscape. Stay up-to-date with the stringent requirements of GMP production, and learn how keeping your quality assurance processes highly specified to your product and isotope can maximize the potential of the raw materials you work with, all while considering IAEA guidance and regional nuances.
Lower the cost per dose of your therapy by reducing wastage and streamlining refining processes, thereby minimizing manufacturing downtime caused by sub-standard quality batches. Our workshop offers you the core principles necessary to tailor your quality assurance process to your specific drug programs. Engage in open and candid discussions with your peers, and learn from industry leaders who are paving the way for the future of radiopharmaceuticals.