Overview: FDA 7348.811 section 1 states, Regardless of the type of system used by the clinical site, the regulatory requirements for clinical data do not change whether clinical data are captured on paper, electronically, or using a hybrid system. What type of system is best for your program and investigator capabilities? The wrong choice yields inspectional non compliance. Price : $139.00 Contact Info: MentorHealth Phone No: 1-800-385-1607 FaX: 302-288-6884 [email protected] Event Link: http://bit.ly/FDA-New-Electronic-Data-Capture-Guidance http://www.mentorhealth.com/

Date : 10th February 2016 to 10th February 2016

Place : United States, Fremont,ca,usa

Website :http://bit.ly/FDA-New-Electronic-Data-Capture-Guidance

Contact Person:Event Manager

Description:

Overview: FDA 7348.811 section 1 states, "Regardless of the type of system used by the clinical site, the regulatory requirements for clinical data do not change whether clinical data are captured on paper, electronically, or using a hybrid system." What type of system is best for your program and investigator capabilities? The wrong choice yields inspectional non compliance. Price : $139.00 Contact Info: MentorHealth Phone No: 1-800-385-1607 FaX: 302-288-6884 [email protected] Event Link: http://bit.ly/FDA-New-Electronic-Data-Capture-Guidance http://www.mentorhealth.com/

Overview: FDA 7348.811 section 1 states, Regardless of the type of system used by the clinical site, the regulatory requirements for clinical data do not change whether clinical data are captured on paper, electronically, or using a hybrid system. What type of system is best for your program and investigator capabilities? The wrong choice yields inspectional non compliance. Price : $139.00 Contact Info: MentorHealth Phone No: 1-800-385-1607 FaX: 302-288-6884 [email protected] Event Link: http://bit.ly/FDA-New-Electronic-Data-Capture-Guidance http://www.mentorhealth.com/ will be held in Fremont,ca,usa,United States on date 2016-02-10

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Deadline for abstracts/proposals : 9th February 2016

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

Conference Highlights :Clinical Research Coordinators and Investigators Medical Record Personnel Clinical CRA Monitors Clinical Program Managers Clinical Quality Assurance Auditors

Venue :Fremont, CA, United States

Check the event website for more details.