TORONTO (PRWEB) OCTOBER 06, 2022
The data characterizing the real-world clinical, economic and humanistic impact of innovative medical products are increasingly used across the broad spectrum of clinical and commercial development to support both regulatory approval and market access (with the former being a relatively new phenomenon since implementation of the 21st Century Cures Act). Despite an increasing number of sources of high-quality real-world data (RWD), there remain many situations in which a data-based solution has important strategic and/or scientific limitations. What are the strategic and scientific imperatives for prospectively generated real-world evidence (RWE)?
Join this webinar to explore the RWE/RWD landscape and the situations in which a prospective observational study or registry presents a more optimal solution, while also focusing on the unique operational factors that must be accommodated to maximize time- and cost-efficiency in the de novo generation of real-world evidence.
Join Jeff Trotter (webinar moderator), Senior Vice President, Scientific Solutions, Real World Evidence, Worldwide Clinical Trials; Mary Glenn Vreeland, Senior Director, Evidence Project Management – United States, Worldwide Clinical Trials; Florence Barkats, CCO and Digital Health & Technology Advisor, Cisiv Ltd.; and Dilesh Doshi, PharmD, Vice President, Global Health Economics and Outcomes Research, Acadia Pharmaceuticals, for the live webinar on Tuesday, October 25, 2022, at 12pm EDT (9am PDT).
For more information, or to register for this event, visit The Strategic and Scientific Imperative for Prospectively Generated Real-World Evidence.
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Contact:
Vera Kovacevic
Tel: +1 (416) 977-6555 x371
Email: vkovacevic@xtalks.com
Source: https://www.prweb.com/releases/the_strategic_and_scientific_imperative_for_prospectively_generated_real_world_evidence_upcoming_webinar_hosted_by_xtalks/prweb18940735.htm