Agent GCP and the Bloody Consent Form GuidebookUniversityOfHealthCare, 2005 - 332 sider Agent GCP is THE way to learn FDA regulations. The exciting, suspenseful, and sometimes zany plot of a murder in a clinical trial is interweaved with interactivity and teaching of FDA regulations in an unforgettable manner. At the completion, learners will have obtained a superb knowledge of informed consent and IRB regulations. This course covers all the regulations on informed consent procedures and Institutional Review Boards (IRBs)—that is, Good Clinical Practices in 45 CFR 46, 21 CFR 50, 21 CFR 56, and other regulations. It is useful for any person or organization participating in clinical trials. The book contains useful aids including a glossary, a list of resources, model consent forms, and texts of regulations. Those readers who wish to have an accompanying program with interactivity should also purchase the CD version. |
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... 21 CFR 50 182 200 213 257 258 259 279 280 301 21 CFR 56 309 Nuremburg Code 316 Declaration of Helsinki 316 Belmont Report 318 Introduction Regulations can be boring. When I had to take Contents Michele's Overview of Good Clinical Practices.
... 21 CFR 50 182 200 213 257 258 259 279 280 301 21 CFR 56 309 Nuremburg Code 316 Declaration of Helsinki 316 Belmont Report 318 Introduction Regulations can be boring. When I had to take Contents Michele's Overview of Good Clinical Practices.
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Vanlige uttrykk og setninger
Access granted access to LEVEL Agency head Agent GCP Answer applicable appropriate Belmont Report blood BRITISH STUDY DOCTOR CARMATE Cheerasil study classified information clinical trial conducted consent form consent process Declaration of Helsinki Department or Agency depression DHHS Drug Administration elements of informed exemption Federal fetus Food and Drug FRENCH CLINICAL INVESTIGATOR Hayworthless Heckle HERETIC individual informed consent document Institutional Review Board intelligence computer displayed investigational new drug investigational product involving human subjects IRB approval IRB review legally authorized representative Level 2 accessed Michele minimal risk NIH MPA Nuremberg Code obtained Office OHSR Oncophrenics Pharmaceutical Corporation patients PEA WHIZ person Pharm Mission Control prisoners Protection of Human Question RACECAR DRIVER Ravennaire Red Raven regulations research activities research involving human research subjects review and approval rights and welfare sponsor subpart System Stroke test article True or false TRUSTWORTHY TY BREAKER VICT