The International Organization for Standardization (ISO) 14155:2020 “Clinical investigation of medical devices for human subjects – Good clinical practice” guideline is an international standard for researching the safety and effectiveness of medical devices. The 2020 edition replaces the earlier version from 2011, with key changes in the responsibilities of sponsors and investigators. This webinar examines the principal revisions of the ISO standard with an eye toward determining how these changes impact the design and execution of clinical trials of medical devices.
Release Date: August 11, 2022
Language Availability: English
Suggested Audiences: Compliance Professionals, Faculty and Post-Docs, General Counsel, Manufacturing Staff, Principal Investigators (PIs), Research Administrators, 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