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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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Code of Federal Regulations: Containing a Codification of Documents of ...

2000
...may require the investigator to provide subjects with a written statement regarding the research. (e) An IRB shall notify investigators and the institution...an opportunity to respond in person or in writing. For investigations involving an exception to informed consent under §50.24 of this chapter, an IRB...
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Code of Federal Regulations: Containing a Codification of Documents of ...

2001
...may require the investigator to provide subjects with a written statement regarding the research. (e) An IRB shall notify investigators and the institution...an opportunity to respond in person or in writing. For investigations involving an exception to informed consent under §50.24 of this chapter, an IRB...
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The Code of Federal Regulations of the United States of America

2002
...waive documentation in accordance with §11.117. Office of the Secretary of Transportation cd) An ERB shall notify Investigators and the institution in...an opportunity to respond in person or in writing. (e) An EBB 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 ...

1996
...shall require documentation of informed consent or may waive documentation in accordance with §11.117. (d) An IRB shall notify investigators and the institution...statement of the reasons for its decision and give the investigs opportunity to respond in perso writing. (e) An IRB shall conduct com review of research...
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The Code of Federal Regulations of the United States of America

1993
...require documentation of informed consent or may waive documentation in accordance with § 97.117. (d) An IRB shall notify investigators and the institution...statement of the reasons for its decision and give the investiga tor an opportunity to respond ic person or in writing. (e) An IRB shall conduct continuing...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1994
...shall require documentation of informed consent or may waive documentation in accordance with 146.117. (d) An IRB shall notify investigators and the institution...notification a statement of the reasons for its decision and grive the investigator an opportunity to respond in person or in writing. (e) An IRB shall conduct...
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Code of Federal Regulations: Containing a Codification of Documents of ...

1988
...National Institutes of Health. Department of Health and Human Services, Bethesda, Maryland 20205. cision to approve or disapprove the proposed research activity,...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 ...

1997
...shall require documentation of informed consent or may waive documentation in accordance with §27.117. (d) An IRB shall notify investigators and the institution...written notification a statement of the reasons for ita decision and give the investigator an opportunity to respond in person or in writing. (e) An IRB...
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The Code of Federal Regulations of the United States of America

1992
...shall require documentation of informed consent or may waive documentation in accordance with 5 11.117. (d) An IRB shall notify investigators and the institution...research activity, it shall include in its written 49 CFR Subtitle A (10-1-92 Edition; notification a statement of the reasons for its decision and give...
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Code of Federal Regulations: Containing a Codification of Documents of ...

2001
...to approve or disapprove the proposed research activity, or of modifications required to secure IBB approval of the research activity. If the IRB decides...an opportunity to respond in person or in writing. (e) An IBB shall conduct continuing review of research covered by this policy at intervals appropriate...
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