PharmaSUG SDE2016presentation·Chicago·Applying CDISC Standards to Clinical Trials: Experience and FeedbackDeconstructing ADRS: Tumor Response Analysis Data Set 09 North America · Chicago, ILSee metadata
PharmaSUG SDE2016presentation·Chicago·Applying CDISC Standards to Clinical Trials: Experience and FeedbackTo IDB or Not to IDB: That is the Question 10 North America · Chicago, ILSee metadata
PharmaSUG SDE2016presentation·Chicago·Applying CDISC Standards to Clinical Trials: Experience and FeedbackADaM Compliance – Starts With Your Specifications 11 North America · Chicago, ILSee metadata
PharmaSUG SDE2016paper·San Diego·Clinical Analysis: Submission and BeyondCreating PDF Annotations for aCRF 02 North America · San Diego, CASee metadata
PharmaSUG SDE2016presentation·San Diego·Clinical Analysis: Submission and BeyondPlan for Success: Strategies for Efficient Development of a High Quality Study Data Reviewer’s Guide 03 North America · San Diego, CASee metadata
PharmaSUG SDE2016presentation·San Diego·Clinical Analysis: Submission and BeyondPreparing ADaM and Related Files for Submission 04 North America · San Diego, CASee metadata
PharmaSUG SDE2016presentation·San Diego·Clinical Analysis: Submission and BeyondThe Study Data Standardization Plan as a Strategic Tool for Analysis & Reporting 05 North America · San Diego, CASee metadata
PharmaSUG SDE2016paper·San Diego·Clinical Analysis: Submission and BeyondLinking Healthcare Claims and Electronic Health Records (EHR) for Patient Management - Diabetes Case Study 06 North America · San Diego, CASee metadata
PharmaSUG SDE2016paper·San Diego·Clinical Analysis: Submission and BeyondMeasuring Medication Adherence in Observational Data 07 North America · San Diego, CASee metadata
PharmaSUG SDE2015presentation·Philadelphia·Extending CDISC Standards: Spare Parts and Turbo ChargersData Standards, Considerations and Conventions within the Therapeutic Area User Guides (TAUGs) 01 North America · Philadelphia, PASee metadata
PharmaSUG SDE2015presentation·Philadelphia·Extending CDISC Standards: Spare Parts and Turbo ChargersNew Enhanced Expectations of the Use of Controlled Terminology 02 North America · Philadelphia, PASee metadata
PharmaSUG SDE2015presentation·Philadelphia·Extending CDISC Standards: Spare Parts and Turbo ChargersIt’s All About EPOCH 03 North America · Philadelphia, PASee metadata
PharmaSUG SDE2015presentation·Philadelphia·Extending CDISC Standards: Spare Parts and Turbo ChargersMaximizing the Value and Utility of ADaM for Pharmacokinetic Analyses and Reporting: Much More Than Just ADPC and ADPP 04 North America · Philadelphia, PASee metadata
PharmaSUG SDE2015presentation·Philadelphia·Extending CDISC Standards: Spare Parts and Turbo ChargersWhat is the “ADAM OTHER” Class of Datasets, and When Should it be Used? 05 North America · Philadelphia, PASee metadata
PharmaSUG SDE2015presentation·Philadelphia·Extending CDISC Standards: Spare Parts and Turbo ChargersTo IDB or Not to IDB 06 North America · Philadelphia, PASee metadata
PharmaSUG SDE2015presentation·Philadelphia·Extending CDISC Standards: Spare Parts and Turbo ChargersUsage of OpenCDISC Community Toolset 2.x.x for Clinical Programmers 07 North America · Philadelphia, PASee metadata
PharmaSUG SDE2015paper·Seattle·Solutions to Challenges in Clinical ProgrammingInfrastructure Designed to Maximize Workflow 01 North America · Seattle, WASee metadata
PharmaSUG SDE2015summary·Seattle·Solutions to Challenges in Clinical ProgrammingCompare and Conquer Key SDTM and ADaM Variables 05 North America · Seattle, WASee metadata
PharmaSUG SDE2015presentation·Seattle·Solutions to Challenges in Clinical ProgrammingUtilizing SAS® for Cross-Report Verification in a Clinical Trials Setting 07 North America · Seattle, WASee metadata
PharmaSUG SDE2015presentation·Seattle·Solutions to Challenges in Clinical ProgrammingHandling Interim and Immature Data In a Clinical Trials Setting 08 North America · Seattle, WASee metadata