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Starting January 7th, 2013: Required Training for IRB-01
If
you are involved in research with human subjects, their tissue, or data, you must complete the following three required training requirements. After January 7th IRB-01 will not accept new protocols via the myIRB system unless all of the training has been completed and is up to date.
NOTE: once you have completed the training it takes several business days to process it and have it updated in myIRB.
NOTE: individuals who are registered in myIRB can look up their own training data. Click here for instructions on how to login in to myIRB and see your own training data.
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Required Training name/type |
Frequency |
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Notes:
| 1. |
HIPAA: you must take the RESEARCH version of this training. UF faculty and staff must complete the following course in myUFL: PRV801 for HIPAA & Privacy – Research in myUFL. |
| 2. |
In October 2012 myUFL underwent an upgrade that enables everyone to complete training in the system. As a result, students, Shands employees, VA only employees, and Unaffiliated Investigators may also complete training via myUFL. However, in order to do so they need to have a role added to their profile in PeopleSoft. UF administrators designated the role of non-faculty/staff as "Person of Interest" (POI).
Students should contact the HR Administrator in their college/department to provide them with the "Person of Interest" role.
Shands employees, VA employees, and unaffiliated investigators should contact the Office of Research HR Administrator, Melissa Beatty (352) 392-4803, and request to be registered as a "Person of Interest".
Once the “Person of Interest” role is processed non-faculty/staff can complete the training via myUFL. |
| 3. |
Click here to read the announcement about the new mandatory training requirement. |
| 4. |
VA researchers need to complete CITI training more frequently to comply with VA requirements. Contact the VA Research Service for more information about this and other VA training requirements: (352) 376-1611 extension 4917. |
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If you previously completed NIH or CITI training within the the past calendar year (2012), you do not need to retake the CITI training if you have a copy of your training certificate. Instead you may send IRB-01 a copy of your certificate and we will upload it into the system. Email a copy of the certificate toufirb-l@lists.ufl.edu. |
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Required
Reading for All Researchers & Research Staff
If
you
are involved in research with human subjects, you are
required to read the following documents:
1. Belmont Report: The
Office of Human Research Protections (OHRP) considers
it unethical for anyone involved in human subject research
not to have read the Belmont Report. It describes and
explains the ethical principles that should be followed
by such investigators: respect for persons, beneficence
and justice.
2. Code of Federal Regulations:
All human subject researchers must
read 45 CFR 46. This document is the Federal regulation
that describes the authority and responsibility of Institutional
Review Boards (IRBs) in protecting human subjects.
3.
IRB Policies & Procedures: All researchers
must read and follow the Policies & Procedures for
each IRB they wish to submit research to.
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- IRB-02
Policies & Procedures
- IRB-03
Policies & Procedures
4.
Researcher
Responsibilities: All researchers must read and
observe these responsibilities.
5.
HIPAA
for Reseacher
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