ICH-FDA Good Clinical Practice – Managing Clinical Trials 2015
10 Nov 2015
Webinar
Description
Topics
Informed Consent
The Principles of ICH GCP
Ethics & IRB Responsibilities
HIPPA Compliance
Sponsor Responsibilites
Investigator Responsibilities
CRO Selection
Quality Management
Trial Management
Trial Design/Protocol
Data Handling/Recordkeeping
Investigator Selection
Monitoring
Essential Documents
FDA Warning Letters
Auditing/ Regulatory Authority Inspections
Who should Attend
Clinical Research Associates
Clinical Quality Assurance Professionals
Investigators
Project Managers
GCP-Focused Regulatory Affairs Professionals
Study Coordinators
Past Events
ICH-FDA Good Clinical Practice – Managing Clinical Trials 2015 - 10 Nov 2015, Webinar (55095)
Important
Please, check "ICH-FDA Good Clinical Practice – Managing Clinical Trials" official website for possible changes, before making any traveling arrangements
Event Categories
Government & Global Issues: Law & Regulations
Health & Medicine: Healthcare, Medical device, Pharma
