| What’s
on Our Web Site |
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LLNL-IRB meeting dates, submission
deadlines, contacts, current IRB members, and Federalwide Assurance
#00004274 (exp. date 02/26/06). |
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Links to federal, state, and
agency regulations for human subjects’ protection. |
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Required reading for every
PI who has not previously submitted an IRB protocol for review by
the LLNL IRB. In submitting a protocol form, a PI certifies that he/she
has read this section and will conform to its guidelines. |
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Guidance and instructions
for preparing a protocol package for review, the elements of consent,
and the responsibilities of the researcher. |
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Decision tree for determining
the level of IRB review and steps to secure IRB approval. |
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Link to Human Subjects Research
Training Tutorial. |
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Answers to our most frequently
asked questions. |
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Links to downloadable forms
for review requests. |
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Links to Web resources regarding
the protection of human subjects. |
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Articles and upcoming activities
of interest pertaining to the human subjects research community as
well as changes or additions to our Web site. |
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The Health Insurance Portability
and Accountability Act (HIPAA) imposes special requirements on investigators
who use and/or disclose protected health information (PHI) in research. |
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Search the IRB Web site. |
