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Date & Time:
17 SEP 2019 @ 10:00 AM - 11:30 AM CST
Description:
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.
Presenters:
Diane Wold, Senior Director, Standards Development, CDISC
Fred Wood, Vice President for Consulting Services, TalentMine
Presenters
- Diane Wold, Senior Director, Standards Development, CDISC
- Fred Wood, Vice President for Consulting Services, TalentMine