Webinar | September 13, 2021

Utilize Real World Evidence For More Efficient Trials In A Regulatory Setting

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Without adequate recruitment and retention of clinical trial participants for a randomized controlled trial, the research objective cannot be addressed, and product development can be slowed or stopped. One way to mitigate these challenges and create more efficient clinical development programs is to leverage an external control group built upon historical clinical trial data to replace or augment a control arm in a randomized clinical trial. Watch this webinar to learn best practices around external controls and making data driven trial design decisions in a regulatory setting.

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