Sentence examples for irb documentation from inspiring English sources

NIH's scientific review administrators "can spend a lot of time tracking people down" to ensure the relevant IRB documentation accompanies applications, explains Suzanne Fisher, director of CSR's division of receipt and referral.

Lastly, when biospecimens are identifiable, 100% of institutions would require study information and 75% would require IRB documentation.

When the researcher who collected the biospecimens will collaborate with researchers at another institution to conduct a new study using the existing biospecimens, even when those specimens have been anonymized, 55% of the IRBs would require documentation of IRB authorization by the collaborators' external site(s) and 78% would require submission of information about the new study (Table  3).

Before conducting the surveys, we obtained oral informed consent from all the fellows, and the IRB waived the documentation of informed consent later in the ethical review process.

The IRB waived the requirement for documentation of informed consent for participation in this survey.

The IRB granted a waiver of written documentation of informed consent from all participants because of the retrospective study design.

When biospecimens are coded/de-identified, 43% of IRBs typically would require an information review and 65% would require documentation of the outside institution's IRB authorization.

Respondents were then asked whether their institutions' IRBs would require either 1) submission of information about the proposed study and/or 2) documentation of the outside institution's IRB authorization for the proposed study.

When a researcher wishes only to provide biospecimens to another researcher, and will not be involved in the new study, 29% of IRBs would require any information about the proposed study and 24% would require documentation from the external (receiving) researcher's IRB when the biospecimens are anonymized (Table  3).

The requirement to obtain written documentation of informed consent was waived by the IRBs in accordance with 45 C.F.R. § 46.117 c).

Institutional Review Board IRBB) submission and approval from Quorum Review IRB for the study was secured by DaVita Clinical Research who maintained appropriate documentation and conducted management of the study in accordance with the ethical principles consistent with Good Clinical Practice and applicable regulatory requirements.