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CREC Research Seminar Upcoming Events Calendar
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| Upcoming Seminars |
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Date/Time of Event |
Title/Description |
Credits |
Location |
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Spring 2012 |
2/20/2012
11:00
- 12:00 PM
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Human Subject Research - When is IRB Review Required? A look at Case Studies, Quality Improvement Initiatives, and Other Activities that may Require IRB Review
This session will discuss the regulations and the process of submitting a project to request a determination by the UH IRB as to whether an activity involves human subject research.
Any activities that have the potential to involve humans, living or deceased, or specimens/data obtained from humans must receive a determination from the UHCMC Center for Clinical Research and Technology (CCRT) regarding the nature of the activity and the type of review required by the IRB.
Philip Cola, MA, UH Vice President for Research and Technology will lead the discussion.
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3 |
RB&C Community Room |
Register |
2/22/2012
9:00
- 10:30 AM
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The Nuts and Bolts of Research Documentation
This session will provide an overview of the fundamentals that must be considered concerning research documentation, including, source documentation in clinical research, essential documentation required by ICH-GCP (International Conference on Harmonisation – Good Clinical Practice) and FDA regulations, storage and retention requirements for research data, electronic documentation and tips for organizing and maintaining your research records. |
4 |
WRB 1413 |
Register |
2/22/2012
10:45
- 12:00 PM
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Communication and Collaboration in Resesarch: Tips and Tactics for Investigators, Students and Staff to Enhance Integrity in Research
Whether your research setting involves one faculty member and one student working together, or a laboratory team of ten or more researchers, staff and students, effective communication is going to be a key factor to the overall success of the project. But, just as the science requires careful planning and dedicated hard work, so do the research relationships. This session will provide insights, as well as practical tips and tactics which can help to ensure that all the members of the research team are communicating effectively. |
0 |
WRB 1413 |
Register |
2/22/2012
12:15
- 1:00 PM
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Complying with the NIH Public Access Policy: From Soup to Nuts
This session will cover the four ways to submit articles to PubMed Central to generate a PMCID, and the subsequent linking of that PMCID to the PI's MyNCBI bibliography and the NIH RePORT system. A light lunch will be available for those attending this session. |
0 |
WRB 1413 |
Register |
2/22/2012
1:00
- 2:30 PM
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Animal Research: Working Effectively with IACUC
The overall role of the Institutional Animal Care and Use Committee (IACUC) is to ensure the humane and sensitive care and use of animals in research. This session will focus on the History and Ethics of Animal Research, current regulations and functional tips. We will also provide information and tools for submitting a protocol, training requirements, protocol addenda, continuing review and post approval monitoring. |
0 |
WRB 1413 |
Register |
2/22/2012
2:30
- 3:45 PM
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Commercializing Research: Working with the Technology Transfer Office
The mission of the Technology Transfer Office (TTO) is to lead the successful commercialization of inventions developed at CWRU through licensing to existing businesses or starting new enterprises. During this presentation, TTO staff will discuss what “successful commercialization” is, the steps taken to reach that goal, and what you should consider as your research progresses. Additionally, you can expect answers to your questions on patents, confidentiality agreements, material transfer agreements and how Tech Transfer interfaces with Sponsored Projects Administration. Finally, you will leave the session with practical advice about working with the office. |
0 |
WRB 1413 |
Register |
2/23/2012
2:00
- 3:00 PM
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Submitting a Continuing Review Application to the UH IRB
Do you have questions about what is required to be submitted to the IRB for your continuing review (CR)? This program will include an in-depth review of the elements required for continuing review submissions that are reviewed either by the full IRB or administratively. Tips for preventing a lapse in IRB approval will also be discussed. This session will be lead by Karya Ottey, UH IRB Coordinator.
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0 |
RB&C Community Room |
Register |
3/7/2012
2:00
- 4:30 PM
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Study Visit Workshop
During this interactive session, participants will take
an in-depth look at an example research protocol and
participate in a mock patient visit for a practical look
at what happens before, during and after a clinical
research study visit. Participants will learn how to use
a protocol, how to fill out case report forms (CRFs),
and how to identify and report adverse events. |
0 |
Lakeside 1400, UHCMC |
Register |
3/15/2012
1:00
- 2:30 PM
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Webinar: Ethical Internet Research: Informed Consent Regulations and Realities (presented by PRIM&R)
The goal of this webinar is to explore the application of the regulations to research conducted via the internet.
The following topics will be addressed during this webinar:
- Specific internet research settings and conditions for consent
- How to apply Common Rule regulatory requirements for informed consent to internet research
- Regulatory flexibilities applicable to consent in internet research
- Parental consent and child assent in internet research involving minors
- Sample language for informed consent documents for internet research regarding data security and confidentiality of research-related information
Presenters:
Elizabeth Buchanan, MLIS, PhD
Endowed Chair in Ethics
Director, Center for Applied Ethics
University of Wisconsin-Stout
Laura Odwazny, JD, MA
Senior Attorney
Public Health Division
Office of the General Counsel
DHHS
This webinar will be of interest to anyone involved with internet research in either the biomedical or social and behavioral contexts.
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4 |
WRB 1413 |
Register |
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