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OverviewAn indispensable guide for statistical programmers in the pharmaceutical industry. Statistical programmers in the pharmaceutical industry need to create standardized clinical data using rules created and governed by the Clinical Data Interchange Standards Consortium (CDISC). This book introduces the basic concepts, pharmaceutical industry knowledge, and SAS programming practices that every programmer needs to know to comply with regulatory requirements. Step-by-step, you will learn how data should be structured at each stage of the process from annotating electronic Case Report Forms (eCRFs) and defining the relationship between SDTM and ADaM, to understanding how to generate a Define-XML file to transmit metadata. Filled with clear explanations and example code, this book focuses only on the essential information that entry-level programmers need to succeed. Full Product DetailsAuthor: Todd Case , Yuting TianPublisher: SAS Institute Imprint: SAS Institute Dimensions: Width: 19.10cm , Height: 1.40cm , Length: 23.50cm Weight: 0.626kg ISBN: 9781955977982ISBN 10: 1955977984 Pages: 240 Publication Date: 18 August 2022 Audience: General/trade , General Format: Hardback Publisher's Status: Active Availability: Available To Order ![]() We have confirmation that this item is in stock with the supplier. It will be ordered in for you and dispatched immediately. Table of ContentsReviewsAn Introduction to Creating Standardized Clinical Trial Data with SAS is a new book designed to give programmers a jump start into the regulatory requirements of the pharmaceutical industry. This unique book goes behind the scenes to better explain the mechanics of SDTMs and ADaMs. The book has all CDISC programming solutions with a comprehensive collection of SDTM and ADaM examples including trial summary domains. This approach is ideal for those who are new to CDISC and want a complete picture. Assignments, case report form data, and variable derivations follow CDISC and Control Terminology guidelines. SAS programs follow a good programming style with code annotations to explain logic. Sunil Gupta, SAS/CDISC Consultant, Trainer and Author An Introduction to Creating Standardized Clinical Trial Data with SAS is a new book designed to give programmers a jump start into the regulatory requirements of the pharmaceutical industry. This unique book goes behind the scenes to better explain the mechanics of SDTMs and ADaMs. The book has all CDISC programming solutions with a comprehensive collection of SDTM and ADaM examples including trial summary domains. This approach is ideal for those who are new to CDISC and want a complete picture. Assignments, case report form data, and variable derivations follow CDISC and Control Terminology guidelines. SAS programs follow a good programming style with code annotations to explain logic. Sunil Gupta, SAS/CDISC Consultant, Trainer and Author Author InformationTab Content 6Author Website:Countries AvailableAll regions |