Date :
Place : United States, Fremont,ca,usa
Website :http://bit.ly/1LYRAlv
Contact Person:Event Manager
Description:
Overview: When conducting clinical trials it is important to understand and be able to identify serious adverse events (SAE). These are events that are serious, likely related to the study drug, device, treatment or procedure, and increase risks to participants or others. Serious adverse events are defined by the FDA as "Any adverse experience that places the patient, in the view of the initial reporter, at immediate risk of death from the adverse experience as it occurred, i.e. Price : $139.00 Contact Info: MentorHealth Phone No: 1-800-385-1607 FaX: 302-288-6884 [email protected] Event Link: http://bit.ly/1LYRAlv http://www.mentorhealth.com/Deadline for abstracts/proposals : 3rd December 2015
Organized By :Netzealous -MentorHealth
Keynote Speakers : 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 fo
Venue :Fremont, CA, United States
Check the event website for more details.