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

[ICO]NameLast modifiedSizeDescription

[DIR]Parent Directory  -  
[DIR]activities-that-require-irb-review/30-Oct-2017 17:32 -  
[DIR]additional-req-for-research-involving-the-dod-files/30-Oct-2017 17:32 -  
[DIR]consenting-subjects-who-do-not-read-speak-or-understand-english/30-Oct-2017 17:32 -  
[DIR]drugs-biologics-and-devices/30-Oct-2017 17:32 -  
[DIR]emergency-use-of-an-unapproved-drug-files/30-Oct-2017 17:32 -  
[DIR]equip-files/30-Oct-2017 17:32 -  
[DIR]ethical-guidelines-fed-regs-and-state-statutes/30-Oct-2017 17:31 -  
[DIR]files-for-cmu-irb-reliance/30-Oct-2017 17:32 -  
[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]iacuc-meeting-results/05-Mar-2015 17:24 -  
[DIR]irb-meeting-results-files/05-Mar-2015 17:32 -  
[DIR]nci-cirb-independent-for-use-at-uci/30-Oct-2017 17:32 -  
[DIR]news-briefs-files/30-Oct-2017 17:32 -  
[DIR]pics-for-citi-faq-page/30-Oct-2017 17:32 -  
[DIR]what-is-aahrpp-aahrpp-visit-2011/30-Oct-2017 17:32 -  
[   ]faq-prisoners-in-research.pdf21-Aug-2019 22:29 15K 
[   ]pregnant-women-fetus-neonates-laminated-sheet.pdf21-Aug-2019 22:28 17K 
[   ]control-of-investigational-devices.pdf21-Aug-2019 22:29 18K 
[   ]irbactionoptions.pdf21-Aug-2019 22:29 18K 
[   ]mediciation management administration of investigational medications.pdf21-Aug-2019 22:29 20K 
[   ]coi-laminated-sheet.pdf21-Aug-2019 22:29 22K 
[   ]criteria-irb-approval-laminated-sheet.pdf21-Aug-2019 22:29 23K 
[   ]prisoners-laminated-sheet.pdf21-Aug-2019 22:29 23K 
[   ]categories-of-exempt-human-subjects-research.pdf21-Aug-2019 22:29 24K 
[   ]children-laminated-sheet.pdf21-Aug-2019 22:29 25K 
[IMG]CAREQ_large_transparent.png21-Aug-2019 22:29 25K 
[TXT]EIP-committee-webpage.html21-Aug-2019 22:29 26K 
[TXT]fda-regulatory-criteria.html21-Aug-2019 22:29 27K 
[TXT]extended-irb-approval.html21-Aug-2019 22:29 27K 
[TXT]lead-researcher-eligibility.html14-Apr-2014 23:32 28K 
[TXT]levels of review.html14-Apr-2014 23:32 28K 
[   ]ucop-guidance-on-surrogate-consent-for-research.pdf21-Aug-2019 22:29 28K 
[TXT]ca-health-and-safety-code24178.html21-Aug-2019 22:29 28K 
[   ]device-laminated-sheet.pdf21-Aug-2019 22:29 31K 
[   ]faq-regarding-the-7yr-de-novo-process.pdf21-Aug-2019 22:29 33K 
[   ]assessment-tool.doc21-Aug-2019 22:29 34K 
[   ]decision-making-capacity-tool.doc21-Aug-2019 22:29 34K 
[TXT] Reviewing-Protocols-Online-Sources-Mobile-Devices.html31-Mar-2015 00:07 34K 
[TXT]CITI-faqs-and-registration-instructions.html21-Aug-2019 22:29 34K 
[IMG]peter-button-animate-3.png21-Aug-2019 22:29 34K 
[IMG]peter-button-animate-4.png21-Aug-2019 22:29 34K 
[IMG]rp-banner-image.svg21-Aug-2019 22:29 34K 
[   ]placebo.pdf21-Aug-2019 22:29 34K 
[   ]clinical-trailsgov-fact-sheet.pdf21-Aug-2019 22:29 35K 
[   ]determining-qualifications-and-ind.pdf21-Aug-2019 22:29 43K 
[   ]irb-meeting-calendar-2019.pdf21-Aug-2019 22:29 43K 
[   ]IRB-EIP-form.doc21-Aug-2019 22:29 48K 
[   ]hud-informed-consent-form.doc21-Aug-2019 22:29 48K 
[   ]study-information-sheet.doc21-Aug-2019 22:29 56K 
[   ]ohrp-guidance-approval-conditions.pdf21-Aug-2019 22:28 61K 
[   ]drug-biologic-accountability-log.doc21-Aug-2019 22:29 80K 
[   ]device-accountability-log.doc21-Aug-2019 22:29 80K 
[   ]hipaa-privacy-rule-education-module-for irb.ppt21-Aug-2019 22:29 94K 
[   ]irbchecklistemergencyuse-04-04-13.doc21-Aug-2019 22:29 99K 
[   ]chart-ancillary-committee-review-needed.pdf21-Aug-2019 22:29 101K 
[   ]fda-faq-about-medical-devices.pdf21-Aug-2019 22:29 105K 
[   ]checklist-for-determining-human-research.doc21-Aug-2019 22:29 119K 
[   ]sr-and-nsr-medical-device-studies.pdf21-Aug-2019 22:29 121K 
[   ]certification-of-surrogate-decision-makers.pdf21-Aug-2019 22:28 131K 
[   ]new-state-requirements.ppt21-Aug-2019 22:29 139K 
[   ]irb-member-coi.ppt21-Aug-2019 22:29 141K 
[   ]privacy-confidentiality-hrp.pdf21-Aug-2019 22:28 154K 
[   ]children-subjects.pdf13-Jan-2015 20:36 164K 
[   ]ucop-guidance-on-institutional-conflict-of-interest-in-research.pdf21-Aug-2019 22:29 180K 
[   ]irb-meetings-and-deadlines.pdf21-Aug-2019 22:29 180K 
[   ]Request-Determination-Non-Human-Subjects.doc21-Aug-2019 22:28 188K 
[   ]fda-guidance-determining-if-an-IND-is-needed.pdf21-Aug-2019 22:29 210K 
[TXT]glossary-of-terms.html21-Aug-2019 22:29 220K 
[   ]amp-028.pdf21-Aug-2019 22:29 239K 
[   ]hipaa-education-irbs.ppt21-Aug-2019 22:29 243K 
[   ]children-subjects.ppt21-Aug-2019 22:29 310K 
[   ]categories-of-expedited-human-subjects-research.pdf21-Aug-2019 22:29 324K 
[   ]privacy-vs-confidentiality.ppt21-Aug-2019 22:29 331K 
[   ]belmont-report-basics.ppt21-Aug-2019 22:29 363K 
[IMG]full-aahrpp-accredidation.jpeg21-Aug-2019 22:29 392K 
[   ]prisoners-as-subjects.ppt21-Aug-2019 22:29 409K 
[   ]FWA.ppt21-Aug-2019 22:29 419K 
[   ]new-irb-members.ppt21-Aug-2019 22:29 464K 
[   ]adverse-events-and-unanticipated problems.ppt21-Aug-2019 22:29 522K 
[   ]dod-addendum-2013.pdf21-Aug-2019 22:29 556K 
[   ]investigational-device-exemptions.pdf21-Aug-2019 22:29 1.1M 
[   ]2018-categories-of-exempt-human-subjects-research.rtf21-Aug-2019 22:29 1.2M 
[   ]equip-townhall-revised-common-rule.pdf21-Aug-2019 22:29 3.6M 
[   ]clinicaltrials-prs-and-results-entry.pdf21-Aug-2019 22:29 7.0M