Lead the development of standards
that improve process efficiency while
supporting the scientific nature of
clinical research.
Recognize the ultimate goal of creating
regulatory submissions that allow for
flexibility in scientific content and
are easily interpreted, understood,
and navigated by regulatory reviewers.
Acknowledge that the data content,
structure and quality of the standard
data models are of paramount importance,
independent of implementation strategy
and platform.
Maintain a global, multidisciplinary,
cross-functional composition for CDISC
and its working groups.
Work with other professional groups
to encourage that there is maximum sharing
of information and minimum duplication
of efforts.
Provide educational programs on CDISC
standards, models, values and benefits.
Accomplish the CDISC goals and mission
without promoting any individual vendor
or organization.
