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SASInstitute A00-282 Exam Syllabus Topics:

SASInstitute Clinical Trials Programming Using SAS 9.4 Sample Questions:

1. Identify the CDISC model with the following characteristics:
XML-based content and format standard facilitates the archive and interchange of the metadata and data for clinical research provides an accurate audit trail that is 21 CRF Part II compliant

A) Trial Design Model (TDM)
B) Operational Data Model (ODM)
C) Study Data Tabulation Model (SDTM)
D) Analysis Data Model (ADaM)

2. Given the following data set WORK.DM:

Which subjects will appear in the LOG file?

A) 003 and 004
B) 004 and 006
C) 001 and 004
D) 001 and 006

3. What is the main focus of Good Clinical Practices (GCP)?

A) harmonized data collection
B) standard monitoring practices
C) protection of subjects
D) standard analysis practices

4. Which statement correctly describes an aspect of a Phase II clinical trial?

A) designed to assess how well the drug works
B) randomized controlled multicenter trials on large patient groups
C) in vitro and in vivo experiments using wide-ranging doses of the drug
D) designed to assess the pharmacovigilance, pharmacokinetics, and pharmacodynamics of a drug

5. This question will ask you to provide a line of missing code.

Which statement must be added to the following program to create a page break in the report after each RACE grouping?

A) break after race;
B) break after race / page;
C) break race / page;
D) break page / race;

Solutions: