Shannon Labout, CCDM, Director, Data ManagementGuest Speaker atSoCRA Phoenix Chapter MeetingWhat We Need To Know About CDISC StandardsPhoenix, AZ, June 4, 2013 – What are CDISC Standards? Will CDISC Standards be required forFDA Submission? How does this affect the clinical research team? Shannon Labout will answer thesequestions 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 healthcaretechnologies, project management and clinical research. She has managed clinical data managementteams in both the U.S. and Europe, and has participated in CRF standardization, and contributed to datastandards development, harmonization and implementation at multiple global pharmaceuticalorganizations and CROs for more than a decade. She has been an active member and team lead on theCDASH team since 2006 and on the SDS team since 2007. Shannon is the past Senior Director ofEducation at CDISC, and has been training on CDISC standards in North America, Europe and Asiasince 2007.The Society of Clinical Research Associates, Inc. is a non-profit, professional organization dedicated tothe continuing education and development of clinical research professionals. The SoCRA PhoenixChapter is a forum for anyone interested or working in clinical research. Visit www.socra.org for moredetails.About SDCStatistics & Data Corporation (SDC) delivers leading-edge statistical analysis and data managementservices to pharmaceutical, biotechnology, and medical device companies, as well as CRO partners. Withbiostatistics and data management expertise at our core, SDC also provides scalable full service clinicaltrial outsourcing via our diverse and complementary strategic partnerships. Speak with us today abouthow SDC will take ownership of your clinical project needs – www.sdcclinical.com.