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History
- Received for publication October 28, 2021
- Revision received January 4, 2022
- Published online June 30, 2022.
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- previous version (January 20, 2022 - 11:56).
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© 2022 by the Society of Nuclear Medicine and Molecular Imaging.
Author Information
- Sue Bunning1,
- Christopher Ignace2,
- Steve Mattmuller3,
- Sally W. Schwarz4,
- Peter J.H. Scott5,
- Henry F. VanBrocklin6,
- Steven S. Zigler7,
- on behalf of the Coalition of Drug Manufacturers
- 1Medical Imaging and Technology Alliance, Arlington, Virginia;
- 2Cardinal Health, Dublin, Ohio;
- 3Kettering Medical Center, Kettering, Ohio;
- 4Department of Radiology, Washington University School of Medicine, St. Louis, Missouri;
- 5Department of Radiology, University of Michigan, Ann Arbor, Michigan;
- 6University of California San Francisco, San Francisco, California; and
- 7Siemens PETNET Solutions, Knoxville, Tennessee
- For correspondence or reprints, contact Peter J.H. Scott (pjhscott{at}umich.edu).
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- Article
- Abstract
- OPENING REMARKS
- SESSION I: CONSIDERATIONS AND TRENDS IN INSPECTIONS AND COMPLIANCE
- SESSION II: LIFE CYCLE MANAGEMENT OF PET DRUG APPLICATIONS
- SESSION III: CHEMISTRY AND PRODUCT QUALITY ASSURANCE
- SESSION IV: CHANGING LANDSCAPE OF PET DRUGS, LABELING REQUIREMENTS, AND ELECTRONIC FILING REQUIREMENTS
- CLOSING REMARKS
- DISCUSSION: WORKSHOP SUMMARY AND RECOMMENDATIONS FROM PET MANUFACTURING STAKEHOLDERS
- CONCLUSION
- DISCLOSURE
- ACKNOWLEDGMENTS
- Footnotes
- REFERENCES
- Figures & Data
- Supplemental
- Info & Metrics
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