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" IRB shall require documentation of informed consent or may waive documentation in accordance with §46.117. (d) An IRB shall notify investigators and the institution in writing of its decision to approve or disapprove the proposed research activity, or... "
The Code of Federal Regulations of the United States of America - Side 20
2004
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The Code of Federal Regulations of the United States of America

2000
...shall require documentation of informed consent or may waive documentation in accordance with §27.117. (d) An IRB shall notify investigators and the Institution...secure IRB approval of the research activity. If the ШВ decides to disapprove a research activity, it shall Include In its written notification a statement...
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The Code of Federal Regulations of the United States of America

2002
...activity, or of modifications required to secure IRB approval of the research activity. If the IBB decides to disapprove a research activity, it shall...an opportunity to respond in person or in writing. (e) An IRB shall conduct continuing review of research covered by this policy at intervals appropriate...
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The Code of Federal Regulations of the United States of America

1998
...documentation of informed consent or may waive documentation In accordance with §745.117. (d) An 1KB shall notify Investigators and the institution in...secure IRB approval of the research activity. If the ГОВ decides to disapprove a research activity, it shall include in its written notification a statement...
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Code of Federal Regulations: Containing a Codification of Documents of ...

2000
...shall require documentation of informed consent or may waive documentation in accordance with §27.117. (d) An IRB shall notify investigators and the institution...research activity, or of modifications required to secure ERB approval of the research activity. If the IRB decides to disapprove a research activity, it shall...
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The Code of Federal Regulations of the United States of America

2006
...require documentation of informed consent or may waive documentation in accordance with §219.117. (d) An IRB shall notify investigators and the institution...research activity, or of modifications required to secure ШВ approval of the research activity. If the IRB decides to disapprove a research activity, it shall...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1999
...documentation of informed consent or may waive documentation in accordance with §690.117. (d) An IBB shall notify investigators and the institution in...research activity, or of modifications required to secure ERB approval of the research activity. If the IRB decides to disapprove a research activity, it shall...
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Code of Federal Regulations: Containing a Codification of Documents of ...

2000
...documentation of informed consent or may waive documentation in accordance with §lc.ll7. (d) An IBB shall notify investigators and the institution in...research activity, or of modifications required to secure IBB approval of the research activity. If the IBB decides to disapprove a research activity, it shall...
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Protecting Human Subjects: First Biennial Report on the Adequacy and ...

United States. President's Commission for the Study of Ethical Problems in Medicine and Biomedical and Behavioral Research - 1981 - 271 sider
...in addition to that specifically mentioned in § 46.116, be given to the subjects when in the IRB 's judgment the information would meaningfully add to...an opportunity to respond in person or in writing. (e) An IRB shall conduct continuing review of research covered by these regulations at intervals appropriate...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1983
...modifications in (to secure approval), or disapprove all research activities covered by these regulations. (b) An IRB shall require that information given to...an opportunity to respond in person or in writing. (e) An IRB shall conduct continuing review of research covered by these regulations at intervals appropriate...
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The Code of Federal Regulations of the United States of America

1998
...documentation of informed consent or may waive documentation in accordance with §46.117. (d) An IBB shall notify investigators and the institution in...an opportunity to respond in person or in writing. (e) An IRB shall conduct continuing review of research covered by this policy at intervals appropriate...
Uten tilgangsbegrensning - Om denne boken




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