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About Chris Holland

Chris Holland author photo Chris Holland has been a SAS user since 1990. He currently works as a Director of Biostatistics for Amgen and has prior experience heading up biostatistics departments for Sucampo Pharmaceuticals, MacroGenics, and Micromet. He has also worked as a statistical reviewer at the Center for Drug Evaluation and Research in the U.S. Food and Drug Administration. It was there where he served as the technical lead for the SDTM/ADaM Pilot Project review team at FDA, a team of FDA staff involved with assessing the suitability of CDISC standards for meeting the needs of medical and statistical reviewers. Chris continues to be active in the CDISC community, particularly with the Analysis Data Model (ADaM) team. He received an M.S. in Statistics from the University of Virginia and a B.S. in Statistics from Virginia Tech. He is an Accredited Professional Statistician™ by the American Statistical Association.
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Coming Soon!

Coming Soon book cover Implementing CDISC Using SAS: An End-to-End Guide
By Jack Shostak and Chris Holland
Anticipated publication date: Fourth quarter 2012

The Clinical Data Interchange Standards Consortium (CDISC) began in 1997 as a global, open, multidisciplinary, nonprofit organization focused on establishing standards to support the acquisition, exchange, submission and archival of clinical research data and metadata. For decades researchers and programmers have used SAS to analyze, summarize, and report clinical trial data. The first SAS book to deal with CDISC standards, Jack Shostak and Chris Holland’s Implementing CDISC Using SAS: An End-to-End Guide is an all-inclusive guide on how to implement and analyze SDTM and ADaM data and prepare clinical trial data for regulatory submissions. Among the topics covered are: creating and using metadata, implementing and validating SDTM and ADaM, preparing data for regulatory submission, as well as various other topics.

Let me know when this book is available