SEND is an implementation of CDISC’s (Clinical Data Interchange Standards Consortium) SDTM (Study Data Tabulation Model) for nonclinical studies. SEND specifies a standard format for presenting nonclinical study data in a consistent, structured format to enable electronic data review.
Nonclinical data included in regulatory submissions to FDA CDER (Center for Drug Evaluation and Research) must now be in SEND format for all studies and datatypes modeled in SEND.
In the webinar, we will talk about below and our SEND Expert will directly answer your questions.
What you will learn in the webinar:
- What is SEND?
- Impact of SEND Standardization
- Data Visualization with SEND Explorer
- Demo of SEND Explorer