Clinical trials:
Clinical Trails
Clinical Trials Terminology for SAS Programmers
A Simple Solution for Managing the Validation of SAS Programs
Electronic Clinical Data Capture
Pharmaceutical Programming: From CRFs to Tables, Listings and Graphs
SAS Programming in the Pharmaceutical Industry
SASâ Programming Career Choices In The Health Care Industry
Some Statistical Programming Considerations for e-Submission
The Changing Nature of SAS Programming in the Pharmaceuticals Industry
Managing Clinical Trials Data using SAS® Software
Quality Control and Quality Assurance in Clinical Research: SAS
CDISC:
An Introduction to CDISC:
CDISC: Why SAS® Programmers Need to Know
CDISC Implementation Step by Step: A Real World Example
CDISC standards
Supporting the CDISC standards
How to test CDISC Operation data Model (ODM) in SAS
The Use of CDISC Standards in SAS from Data Capture to Reporting
Clinical Data Model and FDA/CDISC Submissions
Creating Case Report Tabulations (CRTs) for an NDA Electronic Submission to the FDA
SDTM-annotated CRFs
Data Integrity through DEFINE.PDF and DEFINE.XML
SAS® and the CDISC (Clinical Data Interchange Standards Consortium)
Implementing an Audit Trail within a Clinical Reporting Tool
The CDISC ODM Study Designer :User Manual
XML Basics for SAS Programmers
Annotation of CRFs:
Trial eCRF Pages
Using SAS to Speed up Annotating Case Report Forms in PDF Format
ANNOTATED CASE REPORT FORM AUTOMATION SYSTEM
Annotated CRF 1: Download(CTN0008_SDTM_annotation_20070413.pdf - 2179Kb) Annotated CRF 2: Download(CTN001_SDTM_ANNOTATION_20070330.pdf - 564Kb) Annotated CRF 3: Download(CTN002_SDTM_ANNOTATION_20070403.pdf - 560Kb)
Study Protocol 1: Download
(NIDA-CTN-0001_Bup_Nx_vs_Clonidine_Inpatient_Protocol_v.5b_112700.pdf - 192Kb)
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Clinical SAS programming has a lead role in SAS industry and taking into consideration all it's points in details,it's really a vast source to know more about Clinical trials,it's different phases etc.
ReplyDeleteit 's very interesting to know all sas clinical trails
ReplyDelete
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