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Recruitment & Study-Related Materials
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Research Participants
What Is an IRB?
Participant FAQs
Contact the IRB
Investigators
Submit a Site
How to Submit
IRB Number
Turnaround Time
Compensation/Reimbursement
Transfer of IRB Oversight
Federally-Funded Studies
Submit a Study
Protocol Guide
Consent Template
How to Submit
IRB Number
Turnaround Time
Board Response
Compensation / Reimbursement
Transfer of IRB Oversight for Studies
Federally-Funded Studies
Electronic Informed Consent (eIC)
Ongoing Review
Recruitment & Study-Related Materials
Amendments
Revised Informed Consent
Changes to Investigator or Site Information
IBs & Package Inserts
Unanticipated Problems
Unanticipated Effects
Deviations and Noncompliance
Study Status Reporting
Emergency Use
Appeal a Decision
Subject Transfers
Responsibilities
Education
Approval
Informed Consent
PCP Notification
Safeguards for Vulnerable Subjects
Site Visits
Translations
HIPAA / PIPEDA
Waivers of Authorization
State/Provincial Privacy Laws
Investigator Noncompliance
Events to Report
Conflict of Interest
Federalwide Assurance
DoD Research
Research Guide
Investigators FAQs
Sponsors/CROs
Submit a Site
How to Submit
IRB Number
Turnaround Time
Compensation/Reimbursement
Transfer of IRB Oversight
Submit FWA Site
Submit a Study
Protocol Guide
Informed Consent Template
How to Submit
IRB Number
Turnaround Time
Board Response
Compensation/Reimbursement
Transfer of IRB Oversight
Federally-Funded Studies
Electronic Informed Consent (eIC)
Ongoing Review
Recruitment & Study-Related Materials
Amendments
Revised Informed Consent
Changes to Investigator or Site Information
IBs and Package Inserts
Unanticipated Effects
Unanticipated Problems
Deviations and Noncompliance
Study Status Reporting
Events to Report
Appeal a Decision
Subject Transfers
Federalwide Assurance (FWA)
DoD Research
Sponsor/CRO FAQs
Institutions
Responsibilities
IAA/Reliance Agreement
Submit a Site
Submit a Study
Transfer IRB Oversight for Sites
Transfer IRB Oversight for Studies
Institution FAQs
Our Company
About Us
Commitment to Compliance
The IRB
Accreditation & Audit History
Careers
Community Partnership
Hours & Holidays
Contacts
Services & Technology
IRB Services
IBC Services
Turnaround Times
Mega Trials
Oncology
Neurology
Phase I Research
Minimal Risk Review
Qualifications
Turnaround Time
Request Minimal Risk
Minimal Risk Review
Exemption Determination
Leftover Specimens
Waivers of Consent
Research in Canada
Device Research
Submit a Device Study
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eConsent (eIC)
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Provision Research Compliance Services
eTools
PDQ: Performance Data Quicklist
Resources
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Research Participants
What Is an IRB?
Participant FAQs
Contact the IRB
Investigators
Submit a Site
How to Submit
IRB Number
Turnaround Time
Compensation/Reimbursement
Transfer of IRB Oversight
Federally-Funded Studies
Submit a Study
Protocol Guide
Consent Template
How to Submit
IRB Number
Turnaround Time
Board Response
Compensation / Reimbursement
Transfer of IRB Oversight for Studies
Federally-Funded Studies
Electronic Informed Consent (eIC)
Ongoing Review
Recruitment & Study-Related Materials
Amendments
Revised Informed Consent
Changes to Investigator or Site Information
IBs & Package Inserts
Unanticipated Problems
Unanticipated Effects
Deviations and Noncompliance
Study Status Reporting
Emergency Use
Appeal a Decision
Subject Transfers
Responsibilities
Education
Approval
Informed Consent
PCP Notification
Safeguards for Vulnerable Subjects
Site Visits
Translations
HIPAA / PIPEDA
Waivers of Authorization
State/Provincial Privacy Laws
Investigator Noncompliance
Events to Report
Conflict of Interest
Federalwide Assurance
DoD Research
Research Guide
Investigators FAQs
Sponsors/CROs
Submit a Site
How to Submit
IRB Number
Turnaround Time
Compensation/Reimbursement
Transfer of IRB Oversight
Submit FWA Site
Submit a Study
Protocol Guide
Informed Consent Template
How to Submit
IRB Number
Turnaround Time
Board Response
Compensation/Reimbursement
Transfer of IRB Oversight
Federally-Funded Studies
Electronic Informed Consent (eIC)
Ongoing Review
Recruitment & Study-Related Materials
Amendments
Revised Informed Consent
Changes to Investigator or Site Information
IBs and Package Inserts
Unanticipated Effects
Unanticipated Problems
Deviations and Noncompliance
Study Status Reporting
Events to Report
Appeal a Decision
Subject Transfers
Federalwide Assurance (FWA)
DoD Research
Sponsor/CRO FAQs
Institutions
Responsibilities
IAA/Reliance Agreement
Submit a Site
Submit a Study
Transfer IRB Oversight for Sites
Transfer IRB Oversight for Studies
Institution FAQs
Our Company
About Us
Commitment to Compliance
The IRB
Accreditation & Audit History
Careers
Community Partnership
Hours & Holidays
Contacts
Services & Technology
IRB Services
IBC Services
Turnaround Times
Mega Trials
Oncology
Neurology
Phase I Research
Minimal Risk Review
Qualifications
Turnaround Time
Request Minimal Risk
Minimal Risk Review
Exemption Determination
Leftover Specimens
Waivers of Consent
Research in Canada
Device Research
Submit a Device Study
Device Resources
eConsent (eIC)
Technology
Provision Research Compliance Services
eTools
PDQ: Performance Data Quicklist
Resources
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12/04 2013
Reporting to the IRB Part 2
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