Conference Details

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/

Date :

Place : United States, Fremont,ca,usa

Website :

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/

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/ will be held in Fremont,ca,usa,United States on date 2015-12-03

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 for more details.

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 
support@mentorhealth.com
Event Link: http://bit.ly/1LYRAlv
http://www.mentorhealth.com/

Views: 669

Venue - Map & Directions