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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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Ethical Considerations for Research Involving Prisoners

Committee on Ethical Considerations for Revisions to DHHS Regulations for Protection of Prisoners Involved in Research, Board on Health Sciences Policy, Institute of Medicine - 2007 - 20 sider
...§46.116. The IRB may require that information, in addition to that specifically mentioned in §46.1 16, be given to the subjects when in the IRB's judgment...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

2002
...to that available on the IRB. These individuals may not vote with the IRB. § 46.108 IRB functions and operations. In order to fulfill the requirements...secure IRB approval of the research activity. If the ERB 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 ...

1993
...(a) An IRB shall review and have authority to approve, require modifications in (to secure approva1), or disapprove all research activities covered by this...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 Gift of Participation: A Guide to Making Informed Decisions about ...

Kenneth Getz - 2007 - 360 sider
...shall require documentation of informed consent or may waive documentation in accordance with Sec. 46.117. (d) An IRB shall notify investigators and...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

2005
...require documentation of informed consent or may waive documentation in accordance with §219.117. (d) An IRB shall notify investigators and the institution...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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Miltary Medical Ethics, Volume 2

...require documentation of informed consent or may waive documentation in accordance with Sec. 219.117. (d) An IRB shall notify investigators and the institution...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

1996
...documentation of informed consent or may waive documentation in accordance with §26.117.(d) An ШВ 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...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1992
...shall require documentation of informed consent or may waive documentation in accordance with §60.117. (d) An IRB shall notify investigators and the institution...research activity, it shall include in its written §60.111 notification a statement of the reasons for its decision and give the investigator an opportunity...
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The Code of Federal Regulations of the United States of America

1996
...require documentation of informed consent or may waive documentation in accordance with §745.117. (d) An IRB shall notify investigators and the institution...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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The Code of Federal Regulations of the United States of America

1994
...activity, or of modifications required to secure IRB approval >f the research activity. If the IRB de:ides to disapprove a research activity, it shall include...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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