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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 - Página 18
2004
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Code of Federal Regulations: Containing a Codification of Documents of ...

1999 - 692 páginas
...addition 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...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

1993 - 616 páginas
...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...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

1993 - 592 páginas
...of the IRB are present, including at least one member whose primary concerns are in nonscientif ic areas. In order for the research to be approved, it...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 ...

1995 - 612 páginas
...be approved, It shall receive the approval of a majority of those members present at the meeting. I 46.109 IRB review of research. (a) An IRB shall review...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 ...

2002 - 748 páginas
...approved, it shall receive the approval of a majority of those members present at the meeting. § 46. 109 IRB review of research. (a) An IRB shall review and...an opportunity to respond in person or in writing. (e) An IKB 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 - 668 páginas
...information given to subjects as part of informed consent is In accordance with §46.116. The ШВ may require that information, in addition to that...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 ...

2000 - 724 páginas
...information would meaningfully add to the protection of the rights and welfare of subjects. (c) An IBB shall require documentation of informed consent or...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

2000 - 700 páginas
...shall require documentation of informed consent or may waive documentation in accordance with §26.117. (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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Code of Federal Regulations: Containing a Codification of Documents of ...

1998 - 902 páginas
...require documenta-tion of informed consent or may waive documentation in accordance with §1028.117. (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

2002 - 802 páginas
...shall require documentation of informed consent or may waive documentation in accordance with §16.117. (d) An IRB shall notify investigators and the institution...investigator an opportunity to respond in person or in wiling. (e) An IRB shall conduct continuing review of research covered by this policy at intervals...
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