-
Date and Time:
THU, 4 FEB 2021, 11:00 AM - 12:30 PM Eastern US Standard Time
Description :
Join CDISC as we go over the COVID-19 Therapeutic Area User Guide for Public Review. CDISC relies on the expertise of the research community to ensure neutral, consensus-based standards are developed and adopted by a diverse global community interested in improving clinical research.
In March 2020, CDISC launched a team to rapidly develop guidance on standardizing COVID-19 research data. Due to the public health significance of COVID-19, CDISC assembled a task force of participants from industry, the U.S. Food and Drug Administration (FDA), the U.S. National Institutes of Health (NIH), the World Health Organization (WHO), and academia and expedited the CDISC Standards Development Process to develop and release an Interim User Guide for COVID-19 in three and half weeks. Since the process was expedited, CDISC is now providing the user community the opportunity to provide feedback as part of CDISC's Standards Development Process.
Presenters:
Rebecca Baker, Standards Developer, CDISC
Kit Howard, Sr. Director, Standards Development & Education, CDISC
Bess LeRoy, Head of Standards Development, CDISC
Jon Neville, Sr. Standards Developer, CDISC
Alana St. Clair, Project Manager, CDISC
Diane Wold, Sr. Director, Standards Development, CDISC
Webinar Language: English
Language: English