Investigator Reporting Responsibilities - OHRP

Date : 18th May 2018 to 18th May 2018

Place : United States, Fremont

Website :http://www.compliance4all.com/control/w_product/~product_id=501856LIVE?channel=allconferencealerts_May_2018_SEO

Contact Person:Event Manager

Description:

Overview: The webinar will also discuss how to make determinations of whether an adverse event is probably related, possibly related, or possibly/probably not related to a drug or device. Why should you Attend: Are you being cited for failure to report safety information, changes to the research plan, or protocol deviations/violations or noncompliance to the sponsor or the IRB?

Investigator Reporting Responsibilities - OHRP will be held in Fremont,United States on date 2018-05-18

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Deadline for abstracts/proposals : 17th May 2018

Keynote Speakers :

Venue :Fremont, CA, USA

Check the event website for more details.