This webinar focuses on the FDA inspection process, the role of the FDA Form 483, and what it means for a clinical investigator or research site to receive one. The webinar provides important information to help investigators and sites implement remediations and plan for long term success at the site. It concludes by explaining the required actions with respect to the FDA post 483.
Release Date: March 31, 2022
Language Availability: English
Suggested Audiences: Clinical Investigators, Compliance Professionals, Contract Research Organizations (CROs), IRB Members, Research Administrators, Researchers, Sponsors
Organizational Subscription Price: $300 per year/per site or included as part of an annual subscription to our All Access Webinar Package
Independent Learner Price: $49 per person