Date/Time of Event |
Title/Description |
Credits |
Location |
|
Fall 2009 |
11/23/2009
1:00
- 3:00 PM
|
UHCMC IRB – iRIS – Submitting a New Study
During this interactive session, participants will learn how to use iRIS to submit a new study to the UHCMC IRB. Each participant will have a computer workstation and can create a mock study to submit to the IRB, while following along with the instructor.
Detailed instruction will be provided for submitting a new study to the UHCMC IRB, including completing the application, attaching documents for your submission packet and routing the submission for proper signoff.
Space is limited, please register early!
|
0 |
School of Medicine - E324 |
Register |
11/25/2009
2:30
- 3:00 PM
|
Introducing the UHCMC IRB Electronic Submission System: iRIS
This informational session will provide an overview of the new electronic IRB system that will be implemented, iRIS. General information about the system will be provided along with the rollout timeline and how you can obtain training in the new system.
|
0 |
Lakeside 1400, UHCMC |
Register |
11/30/2009
1:30
- 2:00 PM
|
Introducing the UHCMC IRB Electronic Submission System: iRIS
This informational session will provide an overview of the new electronic IRB system that will be implemented, iRIS. General information about the system will be provided along with the rollout timeline and how you can obtain training in the new system. |
0 |
Lakeside 1400, UHCMC |
Register |
12/1/2009
11:30
- 12:00 PM
|
Introducing the UHCMC IRB Electronic Submission System: iRIS
This informational session will provide an overview of the new electronic IRB system that will be implemented, iRIS. General information about the system will be provided along with the rollout timeline and how you can obtain training in the new system. |
0 |
Lakeside 1400, UHCMC |
Register |
12/2/2009
9:00
- 10:30 AM
|
Preparing for the Unexpected: Pre- and Post-IRB Approval
Isabel Sanchez-Cummings, Director of the Case Behavioral and Social Sciences IRB, will present this seminar which will help researchers anticipate what they need to submit to the IRB for initial approval, even when some aspects of the study are not yet clearly defined. Once the study is approved, direction will be given to guide researchers through the steps they can follow to stay in compliance with their approved protocol when confronted with unexpected challenges during project implementation. |
4 |
BRB 105 |
Register |
12/2/2009
4:00
- 4:30 PM
|
Introducing the UHCMC IRB Electronic Submission System: iRIS
This informational session will provide an overview of the new electronic IRB system that will be implemented, iRIS. General information about the system will be provided along with the rollout timeline and how you can obtain training in the new system. |
0 |
Lakeside 1400, UHCMC |
Register |
12/3/2009
2:00
- 4:00 PM
|
UHCMC IRB – iRIS – Other Submissions (Amendments, AEs, CRs, etc.)
During this interactive session, participants will learn how to use iRIS to submit an amendment, continuing review, adverse event or other submission to the UHCMC IRB. Each participant will have a computer workstation and follow along with the instructor to understand how to submit an amendment, continuing review, adverse event notification, or other submission forms. Attendees in this session should have previous experience working with iRIS or have attended the ‘Submitting a New Study’ session.
Space is limited, please register early!
|
0 |
School of Medicine - E324 |
Register |
12/4/2009
10:00
- 12:15 PM
|
The Use of Placebos in Research
John S. March, MD, MPH, Professor of Psychiatry and Chief of Child and Adolescent Psychiatry at Duke University Medical Center will present the main lecture. Dr. March has extensive experience developing and testing the efficacy and effectiveness of cognitive-behavioral and pharmacological treatments for pediatric mental disorders and will discuss the controversies and considerations related to the use of placebos in research.
A panel discussion with local researchers will follow. |
6 |
WRB 1413 |
Register |
12/7/2009
1:00
- 2:00 PM
|
UHCMC IRB – iRIS – Investigator Signoff
During this interactive session, participants will learn how to use iRIS to complete principal investigator functions within the system. Each participant will have a computer workstation and follow along with the instructor to understand how you will be notified there is a submission waiting for signoff as well as how to review, signoff and submit the study to the UHCMC IRB.
Space is limited, please register early!
|
0 |
School of Medicine - E324 |
Register |
12/7/2009
2:00
- 3:00 PM
|
UHCMC IRB – iRIS – Investigator Signoff
During this interactive session, participants will learn how to use iRIS to complete principal investigator functions within the system. Each participant will have a computer workstation and follow along with the instructor to understand how you will be notified there is a submission waiting for signoff as well as how to review, signoff and submit the study to the UHCMC IRB.
Space is limited, please register early!
|
0 |
School of Medicine - E324 |
Register |
12/9/2009
1:00
- 3:00 PM
|
UHCMC IRB – iRIS – Submitting a New Study
During this interactive session, participants will learn how to use iRIS to submit a new study to the UHCMC IRB. Each participant will have a computer workstation and can create a mock study to submit to the IRB, while following along with the instructor.
Detailed instruction will be provided for submitting a new study to the UHCMC IRB, including completing the application, attaching documents for your submission packet and routing the submission for proper signoff.
Space is limited, please register early!
|
0 |
School of Medicine - E324 |
Register |
12/11/2009
9:00
- 10:30 AM
|
Research Best Practices Part I: General Principles
Puzzled about how to manage all that data? Unsure of authorship standards? Are there expectations and rules for mentors and mentees?
Tracy Wilson-Holden from Case's Office of Research Compliance, will outline important topics such as data management, authorship, collaborative research, peer review, research misconduct and mentoring. Relevant local and federal policies and procedures will be discussed and supplemented with practical examples of real research dilemmas encountered in each area. |
0 |
WRB 1413 |
Register |
12/11/2009
10:45
- 12:15 PM
|
Research Best Practices Part II: Human Studies
Carol Fedor and Cristina Ferrazanno-Yaussey from the Office of Research Compliance & Education at University Hospitals Case Medical Center, will discuss the top non-compliance findings identified through monitoring of clinical research conduct. Helpful tips and tools will be provided to help research teams prevent these significant findings. |
4 |
WRB 1413 |
Register |
12/11/2009
1:00
- 3:00 PM
|
Research Best Practices Part III: Financials
AVP for Research, Diane Domanovics, and the staff from the Sponsored Projects Administration Pre- and Post-Award Offices at Case will present this insightful overview of problem areas identified throughout the entire grant funding process from applying for funding through the spending of awards. Helpful tips and tools will be provided to help research teams navigate the process smoothly and avoid common mistakes that can cause delays. Areas covered include: pre-award processes, project monitoring, cost transfers and closeouts.
|
0 |
WRB 1413 |
Register |
12/14/2009
1:00
- 3:00 PM
|
UHCMC IRB – iRIS – Other Submissions (Amendments, AEs, CRs, etc.)
During this interactive session, participants will learn how to use iRIS to submit an amendment, continuing review, adverse event or other submission to the UHCMC IRB. Each participant will have a computer workstation and follow along with the instructor to understand how to submit an amendment, continuing review, adverse event notification, or other submission forms. Attendees in this session should have previous experience working with iRIS or have attended the ‘Submitting a New Study’ session.
Space is limited, please register early!
|
0 |
School of Medicine - E324 |
Register |
12/15/2009
10:30
- 11:00 AM
|
Introducing the UHCMC IRB Electronic Submission System: iRIS
This informational session will provide an overview of the new electronic IRB system that will be implemented, iRIS. General information about the system will be provided along with the rollout timeline and how you can obtain training in the new system. |
0 |
Lakeside 1400, UHCMC |
Register |
12/16/2009
1:00
- 2:00 PM
|
UHCMC IRB – iRIS – Investigator Signoff
During this interactive session, participants will learn how to use iRIS to complete principal investigator functions within the system. Each participant will have a computer workstation and follow along with the instructor to understand how you will be notified there is a submission waiting for signoff as well as how to review, signoff and submit the study to the UHCMC IRB.
Space is limited, please register early!
|
0 |
School of Medicine - E324 |
Register |
12/21/2009
1:00
- 3:00 PM
|
UHCMC IRB – iRIS – Submitting a New Study
During this interactive session, participants will learn how to use iRIS to submit a new study to the UHCMC IRB. Each participant will have a computer workstation and can create a mock study to submit to the IRB, while following along with the instructor.
Detailed instruction will be provided for submitting a new study to the UHCMC IRB, including completing the application, attaching documents for your submission packet and routing the submission for proper signoff.
Space is limited, please register early!
|
0 |
School of Medicine - E324 |
Register |
12/28/2009
1:00
- 3:00 PM
|
UHCMC IRB – iRIS – Other Submissions (Amendments, AEs, CRs, etc.)
During this interactive session, participants will learn how to use iRIS to submit an amendment, continuing review, adverse event or other submission to the UHCMC IRB. Each participant will have a computer workstation and follow along with the instructor to understand how to submit an amendment, continuing review, adverse event notification, or other submission forms. Attendees in this session should have previous experience working with iRIS or have attended the ‘Submitting a New Study’ session.
Space is limited, please register early!
|
0 |
School of Medicine - E324 |
Register |
12/30/2009
1:00
- 3:00 PM
|
UHCMC IRB – iRIS – Other Submissions (Amendments, AEs, CRs, etc.)
During this interactive session, participants will learn how to use iRIS to submit an amendment, continuing review, adverse event or other submission to the UHCMC IRB. Each participant will have a computer workstation and follow along with the instructor to understand how to submit an amendment, continuing review, adverse event notification, or other submission forms. Attendees in this session should have previous experience working with iRIS or have attended the ‘Submitting a New Study’ session.
Space is limited, please register early!
|
0 |
School of Medicine - E324 |
Register |
