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| A Guide for the Preparation of Applications for Authorization of Positron=emitting Radiopharmaceuticlas for Use in Basic Clinical Research Studies | |||
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| 분류 | Radiopharmaceuticals, Clinical researh, Guidance | 조회 | 2377 |
| 발행년도 | 2014 | 등록일 | 2015-10-02 |
| 출처 | Health Canada (바로가기) | ||
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This Guidance document provides information on the interpretation and application of sections C.03.301 to C.03.320 of the Food and Drug Regulations (the Regulations) applicable to positron-emitting radiopharmaceuticals (PERs) used in basic clinical research studies.
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 이전글 |
Safety in Magnetic Resonance Imaging |
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 다음글 |
Cyclotron Produced Radionuclides: Guidance on Facility Design and Production of [F-18]Fluorodeoxyglucose(FDG) |
