THE COMMUNITY ARCHIVE

Clinical Programming Papers and PresentationsPage 51

Clinical programming connects study data, standards, analysis and reporting. Explore implementation papers on clinical trials, validation and repeatable workflows, then follow a focused topic for a particular dataset or deliverable.

1,393 papers · Showing 1001–1020

PharmaSUG · 2013Paper MS02PharmaSUG 2013

Life Cycle of a Data Point – A Tool to Educate the Clinical Development Team on What it Takes to Go From the Clinic to a Submission

Arthur Collins; Joanna Koft

Source category: Management and Support

Author collections: Arthur Collins · Joanna Koft

PHUSE · 2013Paper AD05PHUSE EU Connect 2013

Organising Deliverables for Clinical Trials - The Concept of Analyses and its Implementation in EXACT

Hansjorg Frenzel

Source category: Applications and Software Development

Author collections: Hansjörg Frenzel

PHUSE · 2013Paper TS09PHUSE EU Connect 2013

Patient Cloud and the Future of Clinical Trials

Christopher Temme

Source category: Technical Solutions

PHUSE · 2013Paper PP03PHUSE EU Connect 2013

Reporting on Oracle Clinical by JReview

Fleury Randrianarivo

Source category: Poster Presentation

PharmaSUG · 2013Paper IB10PharmaSUG 2013

SAS® Programmer to Clinical SAS Programmer

Gayatri Karkera; Neha Mohan

Source category: Industry Basics

Author collections: Gayatri Karkera · Neha Mohan

PharmaSUG · 2013Paper PO15PharmaSUG 2013

SQL Subqueries: Usage in Clinical Programming

Pavan Vemuri

Source category: Posters

Author collections: Pavan Vemuri

PHUSE · 2013Paper PP11PHUSE EU Connect 2013

Standards for the Management of Clinical Trial Data, Why are they Needed, What is Needed?

Isabelle Abousahl

Source category: Poster Presentation

SAS Global Forum · 2013Paper 380-2013SAS Global Forum 2013

Statistical Graphics for Clinical Research Using ODS Graphics Designer

Wei Cheng, Isis Pharmaceuticals, Inc.

Source category: Reporting and Information Visualization

PharmaSUG · 2013Paper BB01PharmaSUG 2013

The Hash of Hashes as a “Russian Doll” Structure: Application to Clinical Adverse Events Data Analysis

Joseph Hinson

Source category: Beyond the Basics

Author collections: Joseph Hinson

PharmaSUG · 2013Paper IB05PharmaSUG 2013

The Value of an Advanced Degree in Statistics as a Clinical Statistical SAS Programmer

Mark Matthews; Ying (Evelyn) Guo

Source category: Industry Basics

Author collections: Mark Matthews · Ying (Evelyn) Guo

PharmaSUG · 2013Paper CC07PharmaSUG 2013

Tracking the Use of Standard Programs in Clinical Trials

Adel Salem

Source category: Coders Corner

PHUSE · 2013Paper PP06PHUSE EU Connect 2013

Two-way Ticket, Please...All aboard the SAS® Clinical Standards Toolkit 1.5 Express

Lex Jansen

Source category: Poster Presentation

Author collections: Lex Jansen

PHUSE · 2013Paper TS05PHUSE EU Connect 2013

Using a Clinical Data Review Tool in an SAS based Environment

Michael Hersch

Source category: Technical Solutions

PHUSE · 2013Paper PP21PHUSE EU Connect 2013

Using the SAS Intelligence Platform for Clinical Trials Programming

Melissa Martinez

Source category: Poster Presentation

Author collections: Melissa Martinez

PharmaSUG · 2013Paper HT06-SASPharmaSUG 2013

Using the SAS® Clinical Standards Toolkit 1.5 to Import CDISC ODM Files

Lex Jansen

Source category: Hands-On Training

Author collections: Lex Jansen

PHUSE · 2013Paper SD08PHUSE EU Connect 2013

Utilising Data Warehousing to Validate Clinical Trial Projects and to Select and Recruit Patients

Tim Armitage

Source category: Software Demonstrations

PHUSE · 2013Paper TS01PHUSE EU Connect 2013

Visual Approaches for Safety Analysis and Review of Clinical Trials

Valerie Nedbal

Source category: Technical Solutions

Author collections: Valerie Nedbal

PHUSE · 2012Paper AD05PHUSE EU Connect 2012

A Maestro for Our Clinical Data... (Sanofi Clinical Data Warehouse)

Alain Vasseur; Celine Tendero

Source category: Applications and Software Development

Author collections: Alain Vasseur · Celine Tendero

SESUG · 2012Paper PO-02SESUG 2012

A Visual Approach to Monitoring Case Report Form Submission During Clinical Trials

Rebecca Horney, Dept. of Veterans Affairs Cooperative Studies Program Coordinating CenterKaren Jones, Dept. of Veterans Affairs Cooperative Studies Program Coordinating CenterAnnette Wiseman, Dept. of Veterans Affairs Cooperative Studies Program Coordinating Center

Source category: Posters

File inside source ZIP: PO-02.pdf

PharmaSUG · 2012Paper CC12PharmaSUG 2012

An Efficient Method to Create Titles for Multiple Clinical Reports Using Proc Format within A Do Loop

Youying Yu

Source category: Coders’ Corner

Author collections: Youying Yu