RQM+ is a global MedTech service provider focused on accelerating compliance and market success. Through our unparalleled expertise and industry knowledge, we deliver specialized solutions and expedite the journey along the full product lifecycle for Med Device and IVD companies, from concept to commercialization to post-market.

Our portfolio of services enables the delivery of end-to-end solutions across the complete med device product lifecycle, with our: 
• Regulatory and Quality Consulting
• Lab Services (Jordi Labs)
• Clinical Trials
• Reimbursement
• Technology Solutions


RQM+

Join us for a free webinar on the importance and application of Real-World-Evidence (RWE) as we aim 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 Attend**

• 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.
