WEBINAR ON-DEMAND
Real-World Evidence for Regulatory Submissions
With changing industry trends and new legislation, having robust real-world evidence (RWE) for your organization is more important than ever.
In this on-demand webinar, you'll hear from experts as they discuss regulatory submissions and how to select quality data. You'll gain insights into PINC AI™ Applied Sciences RWE and how its quality data, which represents over one billion individual patient encounters, can be fit-for-purpose* for your regulatory use.
Topics of discussion will also include:
- Information about recent RWE legislation, including FDA guidance
- Industry trends and resources for filing regulatory submissions
- Case studies from submitting RWE for regulatory submissions, including learnings and challenges
- Leveraging RWE in clinical trials
SPEAKERS:
Myla Maloney Chief Growth Officer, Premier, Inc., PINC AI™ Applied Sciences |
|
Soumi Saha Senior Vice President of Government Affairs, Premier, Inc. |
CONTACT INFORMATION
Premier is committed to protecting the privacy and security of any personal information you provide to us. By clicking here, you understand and acknowledge that the personal information that you are submitting on this form is subject to Premier's privacy policy.
Privacy Policy