Principles of IRB Review 2017 - Webinar on 2017 Principles of IRB Review
Date2017-05-18
Deadline2017-05-17
VenueOnline Event, USA - United States
KeywordsIRB function webinar; Quality Improvement; Health quality management
Topics/Call fo Papers
Training Options
Duration: 90 Minutes
Thursday, May 18, 2017 | 10:00 AM PDT | 01:00 PM EDT
Overview: This webinar will discuss how IRBs can review research to fulfill the regulatory requirements as well as conduct appropriate and complete ethical review of research protocols. Many examples will be provided distinguishing between what must be done to fulfill the regulatory requirements and what should be done for ethical review. For example, having and completing a checklist may fulfil and even document compliance with regulations, but have the content of those items on the checklist been adequately discussed and issues resolved? The discussion will include issues related to the composition of the IRB, conduct of IRB meetings, criteria for approval of research, evaluation of an individual protocol and voting. In addition other HRPP functions will be discussed including education, evaluation of IRB members and staff, quality improvement and annual review of the HRPP/IRB. Attendees will learn the issues to consider to ensure complete review of protocols, optimal IRB function, regulatory compliance and fulfillment of ethical responsibilities for the protection of human subjects in research.
Why should you Attend: IRBs have the complex task of reviewing research in compliance with human subject regulations and conducting an ethical review of the research. This webinar will help organizations complete both of these functions.
Areas Covered in the Session:
Difference between regulatory review and ethics review
How your HRPP/IRB can perform both functions
Composition of your IRB
Conflicts of Interest of IRB Members
Conduct of IRB meetings
Criteria for Approval of Research
Evaluation of IRB Review of An Individual Protocol
Other HRPP/IRB functions
Documentation
Education
Evaluation of IRB Members and Staff
Quality Improvement and Annual Review
Who Will Benefit:
IRB Staff
Institutional Officials
IRB Managers
IRB Administrators
IRB Coordinators
IRB Chairs
IRB Members
Speaker Profile
Dr. Peter Vasilenko is the President of his HRPP/IRB consulting company, Apex Ethical Services, LLC. Previously, Dr. Vasilenko was the Program Director at the Alion HRPP Accreditation Services program and the Vice President for Accreditation at the Association for the Accreditation of Human Research Protection Programs (AAHRPP)
Price: $139.00
Contact Info:
Netzealous -MentorHealth
Phone No: 1-800-385-1607
Fax: 302-288-6884
Email: support-AT-mentorhealth.com
Website:http://www.mentorhealth.com/
Duration: 90 Minutes
Thursday, May 18, 2017 | 10:00 AM PDT | 01:00 PM EDT
Overview: This webinar will discuss how IRBs can review research to fulfill the regulatory requirements as well as conduct appropriate and complete ethical review of research protocols. Many examples will be provided distinguishing between what must be done to fulfill the regulatory requirements and what should be done for ethical review. For example, having and completing a checklist may fulfil and even document compliance with regulations, but have the content of those items on the checklist been adequately discussed and issues resolved? The discussion will include issues related to the composition of the IRB, conduct of IRB meetings, criteria for approval of research, evaluation of an individual protocol and voting. In addition other HRPP functions will be discussed including education, evaluation of IRB members and staff, quality improvement and annual review of the HRPP/IRB. Attendees will learn the issues to consider to ensure complete review of protocols, optimal IRB function, regulatory compliance and fulfillment of ethical responsibilities for the protection of human subjects in research.
Why should you Attend: IRBs have the complex task of reviewing research in compliance with human subject regulations and conducting an ethical review of the research. This webinar will help organizations complete both of these functions.
Areas Covered in the Session:
Difference between regulatory review and ethics review
How your HRPP/IRB can perform both functions
Composition of your IRB
Conflicts of Interest of IRB Members
Conduct of IRB meetings
Criteria for Approval of Research
Evaluation of IRB Review of An Individual Protocol
Other HRPP/IRB functions
Documentation
Education
Evaluation of IRB Members and Staff
Quality Improvement and Annual Review
Who Will Benefit:
IRB Staff
Institutional Officials
IRB Managers
IRB Administrators
IRB Coordinators
IRB Chairs
IRB Members
Speaker Profile
Dr. Peter Vasilenko is the President of his HRPP/IRB consulting company, Apex Ethical Services, LLC. Previously, Dr. Vasilenko was the Program Director at the Alion HRPP Accreditation Services program and the Vice President for Accreditation at the Association for the Accreditation of Human Research Protection Programs (AAHRPP)
Price: $139.00
Contact Info:
Netzealous -MentorHealth
Phone No: 1-800-385-1607
Fax: 302-288-6884
Email: support-AT-mentorhealth.com
Website:http://www.mentorhealth.com/
Other CFPs
Last modified: 2017-03-30 14:02:54