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Speed vs. Safety: How Regulators Are Sizing Up Evidence Today, Upcoming Webinar Hosted by Xtalks

In this free webinar, the featured speakers will discuss the current regulatory trends and the role of CTAP (Coronavirus Treatment Acceleration Program). Attendees will learn about the strategies to address regulatory concerns in today's COVID environment as well as the lasting impact of COVID-era changes on the clinical trial landscape.


News provided by

Xtalks

Oct 15, 2020, 08:30 ET

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TORONTO, Oct. 15, 2020 /PRNewswire-PRWeb/ -- In drug development, there is always pressure to move quickly, and with today's push to develop treatments and vaccines for COVID, those pressures are exacerbated. From sponsors and investors to investigators and regulators, everyone is trying to balance the dual needs for speed and safety.

The places where they find success are likely to change drug development forever.

The speakers will ground their predictions for the future in the historic response of regulatory bodies to epidemics, then explore recent shifts in the regulatory environment in response to COVID and the resulting new efficiencies in drug development.

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Adopting decentralized trials and embracing real-world data allows COVID (and other) trials to proceed at a time when typical site visits are fraught. Once global regulators are secure that even under these new circumstances, the data are still valid and clean, these processes are likely to be more widely implemented. In the meantime, sponsors should be confident about working closely with regulators to understand potentially shifting requirements and to build a strong regulatory strategy.

The speakers will ground their predictions for the future in the historic response of regulatory bodies to epidemics, then explore recent shifts in the regulatory environment in response to COVID and the resulting new efficiencies in drug development.

Join Linda McBride, Executive Director, Regulatory Affairs and Compliance Regulatory Professionals, a division of Premier Research and Vicki Gashwiler, Executive Director, Specialty Programs, Premier Research in a live webinar on Monday, October 26, 2020 at 11am EDT (3pm GMT/UK).

For more information or to register for this event, visit Speed vs. Safety: How Regulators Are Sizing Up Evidence Today.

ABOUT XTALKS

Xtalks, powered by Honeycomb Worldwide Inc., is a leading provider of educational webinars to the global life science, food and medical device community. Every year thousands of industry practitioners (from life science, food and medical device companies, private & academic research institutions, healthcare centers, etc.) turn to Xtalks for access to quality content. Xtalks helps Life Science professionals stay current with industry developments, trends and regulations. Xtalks webinars also provide perspectives on key issues from top industry thought leaders and service providers.

To learn more about Xtalks visit http://xtalks.com
For information about hosting a webinar visit http://xtalks.com/why-host-a-webinar/

SOURCE Xtalks

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