Follow-Up Mastermind Session: Standardising Dosimetry & Imaging Across Clinical Trial Sites

Attendees will evaluate variations in imaging protocols, dosimetry methodologies, and radiopharmacy workflows across multiple hypothetical trial sites to determine how these differences impact study outcomes

• Highlighting which technical variables have the greatest impact on quantitative imaging, absorbed dose calculations, and patient comparability
• Defining best practices for harmonising imaging acquisition, dosimetry analysis, and radiopharmaceutical preparation across sites
• Producing a practical checklist for improving data consistency and regulatory confidence in multicentre radiopharmaceutical trials