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Titlebook: Chemists’ Views of Imaging Centers; Ali M. Emran Book 1995 Springer Science+Business Media New York 1995 imaging.medical imaging.nuclear m

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21#
發(fā)表于 2025-3-25 06:14:19 | 只看該作者
https://doi.org/10.1007/978-3-319-46551-7xclusively by state government. Although states are independent bodies there are many similarities in their regulatory approaches. Differences in the degree of regulatory control are minimized through use of the Suggested State Regulations for the Control of Radiation and other guidance documents pr
22#
發(fā)表于 2025-3-25 07:54:57 | 只看該作者
23#
發(fā)表于 2025-3-25 13:51:45 | 只看該作者
https://doi.org/10.1007/978-3-319-48998-8(IND) applications and new drug applications (NDA). Most of that is applicable to radiopharmaceutical drugs as well as to non-radioactive drugs. There are some points that are unique to radioactive products, for example, radionuclidic and radiochemical identity and purity and specific activity. This
24#
發(fā)表于 2025-3-25 18:00:25 | 只看該作者
https://doi.org/10.1007/978-3-319-48998-8d for its manufacture, processing, packing, or holding do not conform to current good manufacturing practice...” The Current Good Manufacturing Practice regulations, 21 CFR 210 and 211, or CGMP, convey requirements to ensure that all members of the drug industry, including those who make PET radioph
25#
發(fā)表于 2025-3-25 21:30:21 | 只看該作者
26#
發(fā)表于 2025-3-26 01:25:03 | 只看該作者
,Richard Rolle’s Eremitic Ontology, in pharmacy, medicine, the industry and government (including the FDA). It is the publisher of the . and the .. These texts have been designated official compendia in the Federal Food, Drugs, and Cosmetic Act. The USP Convention is neither a regulatory nor an enforcement body, however, the standard
27#
發(fā)表于 2025-3-26 07:06:21 | 只看該作者
https://doi.org/10.1007/978-3-319-49829-4n Director of the FDA Division of Medical Imaging, Surgical and Dental Products, was called to task during a question and answer period for FDA’s apparent lack of responsiveness in approving the radiopharmaceutical 2-.FDG for use in PET. He patiently explained that the FDA Center for Drug Evaluation
28#
發(fā)表于 2025-3-26 11:26:49 | 只看該作者
J. ?mydke,J. Ajay,F. Remacle,R. D. Levineout what is being discussed. To this end I have chosen four categories that were formally defined by a task group on PET site and facility planning set up by the American Association of Physicists in Medicine (1). It is obvious that there is really a continuum of facilities and the lines of definiti
29#
發(fā)表于 2025-3-26 15:12:20 | 只看該作者
Svetoslav Rashev,David C. Moule inopportune time to promote a diagnostic technique at a seemingly staggering cost, for widespread public acceptance. This note addresses the question: must PET always be “big science”? (1) Our conclusion is simple: it needn’t be. With a realistic institutional self-perception, a hospital can chart
30#
發(fā)表于 2025-3-26 19:58:25 | 只看該作者
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