AVAILABLE ON DEMAND
This webinar explains the importance and application of Real-World-Evidence (RWE) and aims to help MedTech teams go from ideal frameworks to practical realities.
Get clear on the difference between real-world data (RWD) and RWE, including how raw data becomes fit-for-purpose evidence. Learn why RWE matters for decision making and regulatory success, and how to bridge the gap by putting it into practice! You’ll see how traditional and innovative data sources, from surveys and wearables to EHR datasets and claims databases, fit into putting RWE into practice.
We’ll share real-life case studies and examples, as well as addresses common pitfalls to avoid, including data quality, device identification, follow-up, continuity of care, clinician insight, reporting consistency, and establishing clinical causality.
In the end, attendees will leave with clear practical tips and strategies for implementing real-world evidence in their own operations.
Who Should Watch
- Regulatory Professionals
- Clinical Affairs Professionals
- Product and Program Managers
- Health Economics and Reimbursement Professionals
- Post-Market Surveillance and Safety Managers
Learning Objectives
- How real-world evidence can support medical devices
- Current methods of acquiring real-world data and their strengths and weaknesses
- Case study highlighting successful use of real-world evidence to support PMCF
Presenters
- Bethany Chung, PhD, RAC, Director of Technical Solutions and Innovation, RQM+
- Amelia Hufford, PhD, SVP, Clinical and Regulatory Science Operations, 3Aware
A certificate of attendance is available upon request for live attendees.
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