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[DOC File]Requirements for All Protocol Submissions:
https://info.5y1.org/irb-submission-requirements_1_e3c7e3.html
The Initial Submission Form is designed to obtain the information required for IRB review of all human subjects research. Additional information is required when research involves specific populations or procedures. This information is submitted using supplements to the initial submission form.
irb submission checklist

[DOCX File]Tufts HS IRB Guidance: International Research with Human ...
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IRB. SUBMISSION REQUIREMENTS. eCAP is the acronym for the HSS electronic Clinical Application Portal. All of the Services at HSS use eCAP for submission of their clinical research protocols. The eCAP Home Page is accessed via the following links: ...
irb submission process

[DOCX File]VA NEBRASKA-WESTERN IOWA HEALTH CARE SYSTEM
https://info.5y1.org/irb-submission-requirements_1_a8d10e.html
For template recruitment materials submitted by the Sponsor and IRB-approved for study-wide use, insertion of site-specific information (i.e. site name, address, phone number, etc.) does not require separate submission as a site-specific item for IRB approval. Only answer “yes” if you are submitting materials other than the Sponsor’s templates for study-wide use. (Sterling IRB ...
types of irb submissions

[DOCX File]How To Submit an IRB Proposal at Cooper University Hospital
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Subcommittee of Human Studies (IRB) Submission. Guidelines. Rev: Jan 2012. Rev. July 2015. INVESTIGATOR REQUIREMENTS: The Principal Investigator (PI) and Co-PI (who shares in funding) must have a VA staff appointment. Non-funded protocols may have only one Principal Investigator. Principal Investigators are encouraged to make an appointment with the IRB Coordinator by calling …
examples of irb submissions

[DOC File]IRB New Application - Home | University of Colorado ...
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Tufts Health Sciences Checklist: International Research with Human Subjects. Use the following checklist as a guide for submitting an IRB application for international research. For additional information or guidance, please refer to the corresponding document, Tufts Health Sciences IRB Guidance: International Research with Human Subjects. When conducting international research, Tufts and its ...
sample irb application submissions

[DOCX File]The Leading Respiratory Hospital in the Nation
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This checklist is designed to ensure all basic requirements have been included as part of your IRB submission. Applications/Protocols without the following will be returned without review. Reminder: As studies vary greatly in topics and methodologies, the IRB reserves the right to request additional information or clarifications as required. Mark/Address all items. Reminder: Faculty Advisors ...
western irb submission

[DOC File]Registry Study Submission Application - Sterling IRB
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The review performed by the Designated IRB will meet the human subject protection program requirements of applicable regulatory agencies. The Designated IRB will follow its written procedures for the review and oversight of the Research Protocol. The Designated IRB will follow its written procedures for reporting findings and actions, subject complaints, unanticipated problems involving risks ...
irb submission doc

[DOC File]FORM: IRB Reliance Agreement
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To meet Human Subject Protections regulatory requirements and other applicable regulatory requirements, other documents including Institutional Review Board (IRB) approvals are required in accordance with ICH E6 Section 8. In order to have standardization of procedures across the study, adequate documentation is necessary. This guide will identify which documents and steps need to be …
irb submission form

[DOCX File]HSS | Hospital for Special Surgery: US #1 for Orthopedics
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The IRB meeting and submission deadline schedule can be found on Imedris under My Assistant – Review Board Meetings.A system generated notice will be emailed to you when the study is assigned to a particular IRB meeting. The IRB Staff will also contact you with a presentation time one week prior to the scheduled meeting. Principal investigators are strongly encouraged to present their study ...
irb submission checklist

Overview of IRB Process | Research and Compliance | Marquette Un…
2019-06-01 · Institutional Review Board Office. NEW PROTOCOL IRB SUBMISSION CHECKLIST. Part A (completed by Study Team member) Review Appendix A for documents requiring submission. Ensure all information and required documents are included in the submission. Incomplete information or an incomplete submission packet will delay the IRB’s consideration of the study. Part B (completed by …
irb submission process

Irb submission requirements