Investigator Reporting Responsibilities - OHRP
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Website http://www.compliance4all.com/control/w_product/~product_id=501856LIVE?channel=ourglocal_May_2018_SE |
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Category Investigator Reporting Responsibilities, fraud investigator, how to be a private investigator, investigator responsibilities in clinical research, Clinical Research Associates, online regulatory training
Deadline: May 17, 2018 | Date: May 18, 2018
Venue/Country: Online, U.S.A
Updated: 2018-03-20 14:59:47 (GMT+9)
Call For Papers - CFP
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?Areas Covered in the Session:FDA RegulationsOverview of recent changes in regulatory frameworkGCP R2 GuidelinesFDA guidance on electronic source documentationFDA BIMO ProgramQuality Management of DataEnhancing Excellence in conduct of Clinical TrialsWho Will Benefit:Clinical Research InvestigatorsResearch NursesResearch ManagersClinical Research Associates (CRAs)Clinical Research CoordinatorsCompliance OfficersSpeaker Profile:George Gasparis has over 35 years of experience in the administration or conduct of human subjects research.He worked at the Office for Human Research Protections (OHRP) for seven years and served as the Director, Division of Assurances and Quality Improvement from 2000-03, where he led the development of the OHRP QI Program and electronic submission of the Federalwide Assurance (FWA).Event Fee: One Dial-in One Attendee Price: US$150.00Contact Detail:Compliance4All DBA NetZealous,Phone: +1-800-447-9407Email: supportcompliance4All.com
Keywords: Accepted papers list. Acceptance Rate. EI Compendex. Engineering Index. ISTP index. ISI index. Impact Factor.
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