Date & Time:
17 SEP 2019 @11:00 AM -12:30 PM ET
CDISC’s Standard for the Exchange of Nonclinical Data Implementation Guide (SENDIG) contains domains for general toxicology, pharmacology, and carcinogenicity studies. This webinar will address cases where concepts developed for non-clinical trials may be useful for human clinical trials and will provide an insight into non-clinical practices and procedures, with a focus on their similarities and differences.
Diane Wold, Senior Director, Standards Development, CDISC
Fred Wood, Vice President for Consulting Services, TalentMine
Webinar Language: English
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