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.
Today’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.
Bring your questions and join the conversation!
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