SOPs development and implementation, Standardization
Risk-based Quality Management (RBQM)
Who should Attend
Clinical Research Coordinators (CRCs) and Clinical Research Associates (CRAs), Data Managers or others working in Biomedical Product Development and/or interested in transitioning into Clinical Trials Field
Clinical, Regulatory, Research and Department (R&D) Staff who will Design Clinical Trial Programs
Regulatory Affairs
Grant Administrators
Past Events
ICH GCP Guidelines E6 Revision, R2 Addendum- Changes Impacting Sponsors-CRO-Sites 2019 - 15 Jan 2019, Webinar (79515)
Important
Please, check "ICH GCP Guidelines E6 Revision, R2 Addendum- Changes Impacting Sponsors-CRO-Sites" official website for possible changes, before making any traveling arrangements
Event Categories
Education: Education Technologies & Methods, Training
