Understanding GDPR And Its Impact On Clinical Research
Source: Castor
Understanding the GDPR requirements and their impact on clinical research can be quite challenging. Watch an interactive webinar with:
- Caroline Cabezas (Legal Counsel & Privacy Officer at Castor)
- Rahel Meister (Senior Clinical Study Manager at Smith & Nephew)
What you’ll learn:
1. How the GDPR requirements affect clinical research, specifically patient informed consent and data management
2. Data minimization for researchers
3. And lastly, what really happens during a data breach
access the Webinar!
Log In
Get unlimited access to:
Trend and Thought Leadership Articles
Case Studies & White Papers
Extensive Product Database
Members-Only Premium Content
Welcome Back! Please Log In to Continue.
X
Enter your credentials below to log in. Not yet a member of Clinical Leader? Subscribe today.
Subscribe to Clinical Leader
X
Subscribe to Clinical Leader
Castor
This website uses cookies to ensure you get the best experience on our website. Learn more