Research 2013 - Considerations in International Research - Webinar By MentorHealth
Date2013-11-21
Deadline2013-11-21
Venueonline event, USA - United States
Keywordsonline healthcare trainings; Regulatory Compliance; Clinical Research
Websitehttps://bit.ly/1ea97Eo
Topics/Call fo Papers
Overview: More and more researchers are conducting their studies internationally for a variety of reasons. International research can be very beneficial but it can also be costly and time consuming especially when the research is unaware of what should be considered before embarking on such a project.
Why should you attend: Individuals considering conducting research in international settings, mentoring those who will conduct research abroad and those responsible for reviewing or developing the proposals.
Areas Covered in the Session:
International Ethics Committees
Ethical Considerations such as group harms and vulnerability
Embargos
Additional Regulatory Criteria
Cultural Reviews
Practical considerations such as costs and feasibility
Growth in international research
International Ethics Committees
Ethical Considerations such as group harms and vulnerability
Who Will Benefit:
Human Subjects Research
Clinical Research Coordinator positions
Investigator positions
Administration in charge of Clinical Research
Regulatory Compliance
Sarah Fowler-Dixon, PhD, CIP is Education Specialist and instructor with Washington University School of Medicine. She has developed a comprehensive education program for human subject research which has served as a model for other institutions. She crafted budgets, policies, procedures, reporting, and training for the new program. She has initiated the planning, development, authorship and implementation of many human subjects research policies, practices, guidelines, submission and reviewer forms often working with state and federal authorities.
Event Link:http://bit.ly/1ea97Eo
webinars-AT-mentorhealth.com
Phone No: 800-385-1607
FaX: 302-288-6884
Why should you attend: Individuals considering conducting research in international settings, mentoring those who will conduct research abroad and those responsible for reviewing or developing the proposals.
Areas Covered in the Session:
International Ethics Committees
Ethical Considerations such as group harms and vulnerability
Embargos
Additional Regulatory Criteria
Cultural Reviews
Practical considerations such as costs and feasibility
Growth in international research
International Ethics Committees
Ethical Considerations such as group harms and vulnerability
Who Will Benefit:
Human Subjects Research
Clinical Research Coordinator positions
Investigator positions
Administration in charge of Clinical Research
Regulatory Compliance
Sarah Fowler-Dixon, PhD, CIP is Education Specialist and instructor with Washington University School of Medicine. She has developed a comprehensive education program for human subject research which has served as a model for other institutions. She crafted budgets, policies, procedures, reporting, and training for the new program. She has initiated the planning, development, authorship and implementation of many human subjects research policies, practices, guidelines, submission and reviewer forms often working with state and federal authorities.
Event Link:http://bit.ly/1ea97Eo
webinars-AT-mentorhealth.com
Phone No: 800-385-1607
FaX: 302-288-6884
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Last modified: 2013-10-10 14:25:48