1. Shannon Labout, CCDM, Director, Data Management
Guest Speaker at
SoCRA Phoenix Chapter Meeting
What We Need To Know About CDISC Standards
Phoenix, AZ, June 4, 2013 – What are CDISC Standards? Will CDISC Standards be required for
FDA Submission? How does this affect the clinical research team? Shannon Labout will answer these
questions and more in her presentation at the Society of Clinical Research Associates Valley of the Sun
(SoCRA Phoenix) Chapter Meeting on Tuesday, June 4, 2013 in Phoenix, AZ.
Shannon Labout is a Certified Clinical Data Manager (CCDM) with 18+ years experience in healthcare
technologies, project management and clinical research. She has managed clinical data management
teams in both the U.S. and Europe, and has participated in CRF standardization, and contributed to data
standards development, harmonization and implementation at multiple global pharmaceutical
organizations and CROs for more than a decade. She has been an active member and team lead on the
CDASH team since 2006 and on the SDS team since 2007. Shannon is the past Senior Director of
Education at CDISC, and has been training on CDISC standards in North America, Europe and Asia
since 2007.
The Society of Clinical Research Associates, Inc. is a non-profit, professional organization dedicated to
the continuing education and development of clinical research professionals. The SoCRA Phoenix
Chapter is a forum for anyone interested or working in clinical research. Visit www.socra.org for more
details.
About SDC
Statistics & Data Corporation (SDC) delivers leading-edge statistical analysis and data management
services to pharmaceutical, biotechnology, and medical device companies, as well as CRO partners. With
biostatistics and data management expertise at our core, SDC also provides scalable full service clinical
trial outsourcing via our diverse and complementary strategic partnerships. Speak with us today about
how SDC will take ownership of your clinical project needs – www.sdcclinical.com.