Index of /cascade/compliance/human-research-protections/docs

[ICO]NameLast modifiedSizeDescription

[DIR]Parent Directory  -  
[TXT]levels of review.html14-Apr-2014 23:32 28K 
[TXT]lead-researcher-eligibility.html14-Apr-2014 23:32 28K 
[   ]children-subjects.pdf13-Jan-2015 20:36 164K 
[DIR]iacuc-meeting-results/05-Mar-2015 17:24 -  
[DIR]irb-meeting-results-files/05-Mar-2015 17:32 -  
[TXT] Reviewing-Protocols-Online-Sources-Mobile-Devices.html31-Mar-2015 00:07 34K 
[DIR]files-for-special-issues-in-human-subject-research/30-Oct-2017 17:31 -  
[DIR]files-uc-memorandum-of-understanding-for-multi-campus-research/30-Oct-2017 17:31 -  
[DIR]ethical-guidelines-fed-regs-and-state-statutes/30-Oct-2017 17:31 -  
[DIR]drugs-biologics-and-devices/30-Oct-2017 17:32 -  
[DIR]files-for-cmu-irb-reliance/30-Oct-2017 17:32 -  
[DIR]activities-that-require-irb-review/30-Oct-2017 17:32 -  
[DIR]emergency-use-of-an-unapproved-drug-files/30-Oct-2017 17:32 -  
[DIR]consenting-subjects-who-do-not-read-speak-or-understand-english/30-Oct-2017 17:32 -  
[DIR]pics-for-citi-faq-page/30-Oct-2017 17:32 -  
[DIR]nci-cirb-independent-for-use-at-uci/30-Oct-2017 17:32 -  
[DIR]what-is-aahrpp-aahrpp-visit-2011/30-Oct-2017 17:32 -  
[DIR]additional-req-for-research-involving-the-dod-files/30-Oct-2017 17:32 -  
[DIR]news-briefs-files/30-Oct-2017 17:32 -  
[DIR]equip-files/30-Oct-2017 17:32 -  
[   ]faq-regarding-the-7yr-de-novo-process.pdf27-Apr-2018 18:14 33K 
[IMG]full-aahrpp-accredidation.jpeg27-Apr-2018 18:14 392K 
[   ]clinicaltrials-prs-and-results-entry.pdf27-Apr-2018 18:14 7.0M 
[TXT]CITI-faqs-and-registration-instructions.html27-Apr-2018 18:14 33K 
[TXT]fda-regulatory-criteria.html27-Apr-2018 18:14 26K 
[   ]assessment-tool.doc27-Apr-2018 18:14 34K 
[   ]individual-investigator-agreement.doc27-Apr-2018 18:14 41K 
[   ]placebo.pdf27-Apr-2018 18:14 34K 
[   ]coi-laminated-sheet.pdf27-Apr-2018 18:14 22K 
[   ]privacy-confidentiality-hrp.pdf27-Apr-2018 18:14 154K 
[   ]irbchecklistemergencyuse-04-04-13.doc27-Apr-2018 18:14 99K 
[   ]sr-and-nsr-medical-device-studies.pdf27-Apr-2018 18:14 121K 
[   ]ucop-guidance-on-surrogate-consent-for-research.pdf27-Apr-2018 18:14 28K 
[   ]categories-of-expedited-human-subjects-research.pdf27-Apr-2018 18:14 324K 
[   ]criteria-irb-approval-laminated-sheet.pdf27-Apr-2018 18:14 13K 
[   ]irb-authorization-agreement.doc27-Apr-2018 18:14 51K 
[   ]hud-informed-consent-form.doc27-Apr-2018 18:14 48K 
[   ]study-information-sheet.doc27-Apr-2018 18:14 56K 
[   ]irb-member-coi.ppt27-Apr-2018 18:14 141K 
[   ]amp-028.pdf27-Apr-2018 18:14 239K 
[   ]ucop-guidance-on-institutional-conflict-of-interest-in-research.pdf27-Apr-2018 18:14 180K 
[   ]clinical-trailsgov-fact-sheet.pdf27-Apr-2018 18:14 35K 
[   ]fda-guidance-determining-if-an-IND-is-needed.pdf27-Apr-2018 18:14 210K 
[   ]irb-meetings-and-deadlines17.pdf27-Apr-2018 18:15 45K 
[   ]new-irb-members.ppt27-Apr-2018 18:15 464K 
[   ]Request-Determination-Non-Human-Subjects.doc27-Apr-2018 18:15 188K 
[   ]irbactionoptions.pdf27-Apr-2018 18:15 18K 
[   ]IRB-EIP-form.doc27-Apr-2018 18:15 48K 
[   ]ohrp-guidance-approval-conditions.pdf27-Apr-2018 18:15 61K 
[   ]chart-ancillary-committee-review-needed.pdf27-Apr-2018 18:15 98K 
[   ]privacy-vs-confidentiality.ppt27-Apr-2018 18:15 331K 
[   ]FWA.ppt27-Apr-2018 18:15 419K 
[TXT]ca-health-and-safety-code24178.html27-Apr-2018 18:15 28K 
[   ]determining-qualifications-and-ind.pdf27-Apr-2018 18:15 43K 
[   ]certification-of-surrogate-decision-makers.pdf27-Apr-2018 18:15 59K 
[   ]new-state-requirements.ppt27-Apr-2018 18:15 139K 
[TXT]EIP-committee-webpage.html27-Apr-2018 18:15 25K 
[TXT]extended-irb-approval.html27-Apr-2018 18:15 28K 
[   ]dod-addendum-2013.pdf27-Apr-2018 18:15 556K 
[   ]device-laminated-sheet.pdf27-Apr-2018 18:15 31K 
[   ]checklist-for-determining-human-research.doc27-Apr-2018 18:15 119K 
[   ]belmont-report-basics.ppt27-Apr-2018 18:15 363K 
[   ]adverse-events-and-unanticipated problems.ppt27-Apr-2018 18:15 522K 
[TXT]glossary-of-terms.html27-Apr-2018 18:15 219K 
[   ]hipaa-privacy-rule-education-module-for irb.ppt01-May-2018 20:26 94K 
[   ]decision-making-capacity-tool.doc03-May-2018 22:29 34K 
[   ]hipaa-education-irbs.ppt10-May-2018 16:18 243K 
[   ]drug-biologic-accountability-log.doc10-May-2018 16:39 80K 
[   ]mediciation management administration of investigational medications.pdf10-May-2018 16:39 20K 
[   ]device-accountability-log.doc10-May-2018 16:39 80K 
[   ]control-of-investigational-devices.pdf10-May-2018 16:39 18K 
[   ]fda-faq-about-medical-devices.pdf10-May-2018 16:39 105K 
[   ]investigational-device-exemptions.pdf10-May-2018 16:39 1.1M 
[   ]irb-meetings-and-deadlines.pdf14-May-2018 20:41 43K 
[   ]categories-of-exempt-human-subjects-research.pdf15-May-2018 17:59 24K 
[   ]faq-prisoners-in-research.pdf16-May-2018 14:51 15K 
[   ]children-laminated-sheet.pdf16-May-2018 14:51 25K 
[   ]pregnant-women-fetus-neonates-laminated-sheet.pdf16-May-2018 14:51 17K 
[   ]prisoners-laminated-sheet.pdf16-May-2018 14:51 23K 
[   ]children-subjects.ppt16-May-2018 14:51 310K 
[   ]prisoners-as-subjects.ppt16-May-2018 14:51 409K