Investigator Reporting Responsibilities: AEs, Unanticipated Problems, Modifications, and Deviations 2018
18 May 2018
Webinar
Description
Topics
Overview of recent changes in regulatory framework
FDA Regulations
FDA guidance on electronic source documentation
GCP R2 Guidelines
Quality Management of Data
FDA BIMO Program
Enhancing Excellence in conduct of Clinical Trials
Who should Attend
Clinical Research Associates (CRAs)
Research Managers
Compliance Officers
Clinical Research Coordinators
Past Events
Investigator Reporting Responsibilities: AEs, Unanticipated Problems, Modifications, and Deviations 2018 - 18 May 2018, Webinar (75260)
Important
Please, check "Investigator Reporting Responsibilities: AEs, Unanticipated Problems, Modifications, and Deviations" official website for possible changes, before making any traveling arrangements
Event Categories
Education: E-learning, Education Technologies & Methods, Training
Government & Global Issues: Law & Regulations
Health & Medicine: Medical device, Medical laboratories, Medical technology
