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DTSTART;TZID=America/Chicago:20240828T120000
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DTSTAMP:20240904T173823Z
CREATED:20240813T214236Z
LAST-MODIFIED:20240904T173823Z
UID:6301-1724846400-1724849100@criterionedge.com
SUMMARY:Ask the Expert: The Role of Real-World Evidence (RWE) in Regulatory Submissions
DESCRIPTION:Welcome to our Ask The Expert series\, where the Criterion Edge team of experts take your questions on trending industry topics relevant to the work you do every day.  From global regulatory challenges\, clinical evidence issues or regulatory writing best practices\, the goal of this Q&A format is to share information\, ideas and solutions. \nToday’s conversation tackles the rapidly evolving landscape of Real World Evidence and its potential use in global regulatory submissions\, as we discussed in our July 31st Pharma In Focus: The Role of Real World Evidence in Regulatory Submissions webinar. \nBring your questions and join the conversation! \n  \nWATCH WEBINAR
URL:https://criterionedge.com/event/ask-the-expert-the-role-of-real-world-evidence-rwe-in-regulatory-submissions/
LOCATION:Webinar\, United States
ATTACH;FMTTYPE=image/png:https://criterionedge.com/wp-content/uploads/Webinar-8_28_2024-dr-Sheila-Grab-v4.png
ORGANIZER;CN="Criterion Edge":MAILTO:support@criterionedge.com
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