ISO 14155 and FDA Requirements – Trials Conducted at the Research Site
Join this live webinar program as we delve into medical devices and investigational medical devices.
Share your expertise and real-world challenges to improve how trials are conducted for the benefit of everyone.
Participate!Join this live webinar program as we delve into medical devices and investigational medical devices.
This live webinar will challenge attendees to self-reflect on their own leadership practices and how those may be in need of transformation.
Join the Canada Chapter for an open forum to discuss informed consent form implementation and processes.
Clinical trial professionals with an interest or role in the onboarding and education of new staff are encouraged to attend this live webinar and learn valuable best practices from the steps taken, barriers encountered, and resources available during one clinical trial site’s journey toward realizing its goal for optimal efficiency.
Earn your ACRP certification by registering during the Fall 2024 registration window, January 1 - April 30, 2024. ACRP members save on exam preparation and testing fees!