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Good Programming Practice for Clinical Trials by Sunil Gupta
The following are draft recommendations a Good Programming Practice for analysis, reporting and data manipulation in Clinical Trials and the Healthcare industries. The purpose is to encourage...
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SAS Proficiency Test
Here are some common SAS questions: 1- What happens if no VAR statement is used in PROC PRINT? 2- Understand how SAS processes a data step 3- Explain what a (data step) SELECT statement does 4- What is...
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Professional Timeline – Clinical Programmer
Professional Timeline CVFiled under: 21CRF 11, Advanced SAS, Base, Best Practices, Checklists, Clintrial, Cognos, Data Management, Data Mapping, Data Standards, Data Validation, DMP, eClinical, EDC,...
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SAS Date format
What is the date format that will display a SAS date as YYYYMMDD? e.g. 20130815 Use YYMMDDN SAS formatFiled under: Advanced SAS, Base, Data Standards, SAS, Tips Tagged: clinical programming, data...
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CDASH News: More Thoughts from the CDISC Interchange in Sweden
FAIR USE- “Copyright Disclaimer Under Section 107 of the Copyright Act 1976, allowance is made for “fair use” for purposes …Continue reading →
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Did You Know?
Did You Know? » PROC CDISC? It is a new SAS procedure that is available as a hotfix for SAS …Continue reading →
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CDISC/CDASH Standards at your Fingertips
A standard database structure using CDISC (Clinical Data Interchange Standards Consortium) and CDASH (Clinical Data Acquisition Standards Harmonization) standards can …Continue reading →
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Project Plan: CDISC Implementation
CDISC standards have been in development for many years. There are now methodologies and technologies that would make the transformation …Continue reading →
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Solving Data Collection Challenges
Cross-partnership between sponsors and CROs for the collection and analysis of clinical trial data are complex. As a result there …Continue reading →
View ArticleFreelancer / Consultant / EDC Developer / Clinical Programmer
* Setting up a project in EDC (Oracle InForm, Medidata Rave, OpenClinica, OCRDC) * Creation of electronic case report forms (eCRFs) * Validation of programs, edit checks * Write validation test scripts...
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