Name
Medical Devices 101 Breakout: Site Operations for Medical Device Studies
Date & Time
Monday, October 17, 2022, 11:30 AM - 12:15 PM
Location Name
Wilshire AB
Description

Medical device studies might require revisions to your Standard Operating Procedures and policies.

The presentations will focus on the most important requirements for facilities, personnel, and organizational structure.

 

Speakers
Kimberly A. Dorsch - Sr. Director, Clinical Affairs - Hemanext
Angela Rose - VP Clinical Trial Operations - Verici Dx
Kimberly A. Dorsch Angela Rose
Learning Objectives
  1. Identify the scope of site training and impacted departments.
  2. Define device specific contract and documentation requirements.
  3. Explore Post Market Surveillance requirements for Sponsors and leverage your site’s data for Post Market study opportunities.
This Module is Eligible for
ACRP CE Points, CCB Credits, CLE Credits, CME Credits, CNE Credits
ACRP CE Points
0.75