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

Click here to ensure your machine has the necessary requirements to run CDISC webinars (run by LogMeIn).