Avoiding Radiation Toxicity: Understanding Dosimetric Endpoints and Challenges in Radiopharmaceutical Clinical Trials
XTalks
FEBRUARY 13, 2023
A clinical research coordinator (CRC), data coordinator or study nurse may be the first to note a potential MR note or exam finding that must be escalated to the investigator for immediate review. Also, any provider needs to recognize all described adverse events noted in the MR since the last patient study visit.
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