PhUSE Paper SD09. "Overnight" Conversion to SDTM Datasets Ready for SDTM Submission Niels Mathiesen, mathiesen & mathiesen, Basel, Switzerland

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Paper SD09 "Overnight" Conversion to SDTM Datasets Ready for SDTM Submission Niels Mathiesen, mathiesen & mathiesen, Basel, Switzerland ABSTRACT This demonstration shows how legacy data (in any format) is converted to SDTM datasets. Clivax does the job for you - divided in five simple conversion steps: 1) Import of the raw data into the system. 2) Assign critical issues with the help of drag and drop. 3) Integrate the assigned data into the system. 4) Activate the SHARE library and supplement your own SDTM Domains as needed. 5) Export the SDTM You get your SDTM submission delivered express "Overnight", fast and simple without any programmers or programming work involved The presentation will be finished with an overview of the built-in power of Clivax. See how the setup of a study can be made within 4 hours - the SDTM submission included. Clivax offers you the ultimate way to take advantage of the compliance with the CDISC / SDTM standard and get SDTM submission for free. 1. INTRODUCTION FDA is strongly encouraging sponsors to submit data in standard form as a key part of its efforts to continue with advancement of review efficiency and quality. FDA has accepted SDTM datasets since 2004. The Center for Drug Evaluation and Research (CDER) has in the document "CDER Common Data Standards Issues Document" from May 2011 taken the opportunity to give feedback and recommendations regarding the submission of standardized datasets. 2. EASY, SIMPLE, FAST AND COST CONCERNED By the help of the right Software you are helped dramatically in order to be able to generate and submit SDTM datasets. Clivax makes it possible to setup a study within 4 hours - the SDTM submission included. And Clivax is even able to import "Legacy studies" and export the SDTM datasets. Clivax demonstrates that SDTM datasets can be done easy, simple and fast. And you save a lot of time and money. It is the most cost concerned way to produce SDTM datasets. Clivax is the full service Software for Clinical Trials. Instead of using a multiple number of software with Clivax you cover the process from the very beginning to the Submission. (End to End Solution). - One Application instead of five - Setup of new study in one day - SDTM already included - Legacy Converting (express over night) 3. SDTM FOR FREE Clivax is designed for submission as SDTM datasets. Without additional programming work you design your SDTM datasets hit the button and receive your SDTM datasets. Without any additional costs included in the Clivax software package. SDTM submission for free 03.09.2011 SD09.DOC Page 1 of 7

4. LEGACY STUDIES The simple concept of Clivax makes it possible in a extremely simplified process to: IMPORT LEGACY SAS Dataset Clivax EXPORT SDTM Dataset 5. DEMONSTRATIONS For you we have chosen to demonstrate the software live. The most illustrative way is to let it happen in front of your eyes. The JavaScript has been prepared. I can show you following steps: 6. FIVE CONVERSION STEPS The five simple conversion steps are: 1) Import of the raw data into the system. 2) Assign critical issues with the help of drag and drop. 3) Integrate the assigned data into the system. 4) Activate the SHARE library and supplement your own SDTM Domains as needed. 5) Export the SDTM. And before we start the automatic running JavaScript I make a resume 6.1 RAW DATA IMPORT Use the Data from your source - Oracle Clinical etc. Example RawData (SAS format) The same example in XML format 03.09.2011 SD09.DOC Page 2 of 7

Upload Legacy Any critical issue is automatically filtered out and prepared for a "handling". PhUSE 2011 6.2. ASSIGN CRITICAL ISSUES. (DRAG AND DROP) The total critical issues / questions are illustrated and the assignment can be done directly - by using "drag and drop" Example Visits 6.3. INTEGRATE THE ASSIGNED DATA INTO THE SYSTEM. 03.09.2011 SD09.DOC Page 3 of 7

6.4. ACTIVATE THE SHARE LIBRARY Activate the CDISC/SDTM structures. Use the built in "SHARE" and supplement your own SDTM Domains as needed. 6.5. EXPORT THE SDTM Export of the SDTM. The Domain (AE) and the SUPP-Domain (SUPPAE). You choose XML format or SAS format 7. AUTOMATIC RUNNING DEMO For this we will use the prepared FuncUnit scripts. 1. Phuse_Demo01.js 2. Phuse_Demo02.js 3. Phuse_Demo03.js 4. Phuse_Demo04.js 5. Phuse_Demo05.js 8. "OVERNIGHT" Just use the latest version of your data to get the actual SDTM version of your data. The process is ready for you - express delivered "overnight" 03.09.2011 SD09.DOC Page 4 of 7

9. DEFINE.XML Clivax is able to automatically create a first version of define.xml. 10. ADaM (ANALYSIS DATA MODEL) If demanded the Clivax structure makes it possible extend the SDTM export with a ADaM export. 11. CLIVAX AND CDISC SHARE IN ACTION - DEMONSTRATION Demonstration of how you setup a new study within 4 hours. SHARE and Clivax does the job for you and your additional bonus is: SDTM for free The demonstration shows how you make a new study - fast and simple without any programmers or programming work involved. And generate the corresponding SDTM structure without additional work. Print the annotated BlankCRF.pdf out as help for a optimization of the ecrf-design. Fill in test data in the ecrf and print the SDTM for control. You have the total SDTM work done for you without additional work. All based on the "state of the art" web technology. From anywhere and on any device including your ipad. 11.1 DESIGN TOOLS (ecrf) "Drag and drop" your Clinical Trial Input Form In any Language And before any data is filled in make the comprehensive test: - Check immediately the design and functionalities (Preview) - Print the BlankCRF.pdf for approval by the colleges - Check the SDTM export. No adaptions are necessary 03.09.2011 SD09.DOC Page 5 of 7

11.2 ecrf PREVIEW ecrf Preview 11.3 BlankCRF (ANNOTATED) BlankCRF 11.4 ecrf TRANSLATIONS ecrf Translations 03.09.2011 SD09.DOC Page 6 of 7

11.5 DATA MANAGEMENT Data Management 12. COMPLIANT TO FDA 21 CFR PART 11 Clivax comply to FDA 21 CFR Part 11 CONTACT INFORMATION Your comments and questions are valued and encouraged. Contact the author at: Niels Mathiesen mathiesen & mathiesen AG für Informatik Peter Merianstrasse 45 Postfach CH-4002 Basel Mail: Niels.Mathiesen@m-m.ag Web: www.clivax.com www.m-m.ag Tel: +41 61 271 69 42 03.09.2011 SD09.DOC Page 7 of 7