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History
- Received for publication August 28, 2021
- Revision received October 4, 2021
- Published online December 3, 2021.
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© 2021 by the Society of Nuclear Medicine and Molecular Imaging.
Author Information
- 1Department of Clinical Health Sciences, St. Louis University, St. Louis, Missouri;
- 2Center for Quantitative Cancer Imaging, Huntsman Cancer Institute, University of Utah, Salt Lake City, Utah; and
- 3Huntsman Cancer Institute, University of Utah School of Medicine, Salt Lake City, Utah
- For correspondence or reprints, contact Sarah Frye (sarah.frye{at}health.slu.edu).
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- Article
- Abstract
- OVERVIEW OF BASIC TERMS, CONCEPTS, AND PHASES OF CLINICAL TRIALS
- SERIES TOPIC 1: ETHICAL ISSUES IN CLINICAL RESEARCH
- SERIES TOPIC 2: APPLICATION OF GCP TO CLINICAL RESEARCH IN MEDICAL IMAGING
- SERIES TOPIC 3: CROS WITH APPLICATIONS IN CLINICAL IMAGING
- SERIES TOPIC 4: CLINICAL RESEARCH PRIMER—REGULATORY PROCESSES, PARTS I AND II (HOW AND WHEN RADIOPHARMACEUTICALS CAN BE USED AND THE ROLE OF THE IRB)
- SERIES TOPICS 5–7: USE OF IMAGING AGENTS IN THERAPEUTIC DRUG DEVELOPMENT AND APPROVAL, IMAGING AGENT TRIALS, AND IMAGING AGENTS WITH RADIOPHARMACEUTICAL THERAPIES IN CLINICAL TRIALS
- CONCLUSION
- DISCLOSURE
- ACKNOWLEDGMENTS
- Footnotes
- REFERENCES
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