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SASInstitute A00-282 Exam Syllabus Topics:
| Section | Weight | Objectives |
| Macro Programming for Clinical Trials | 15% | |
| Clinical Trials Data Structures | 10% | |
| Apply Statistical Procedures for Clinical Trials | 15% | |
| Report Clinical Trials Results | 10% | |
| Validate Clinical Trial Data Reporting | 20% | |
| Regulatory Submissions | 5% | |
| Clinical Trials Process | 5% | |
| Manage Clinical Trials Data | 5% | |
| Transform or Summarize Clinical Trials Data | 15% | |
SASInstitute Clinical Trials Programming Using SAS 9.4 Sample Questions:
1. What is the primary purpose for specifying identifier variables across SDTM domains?
A) To include the appropriate study information
B) To satisfy regulatory conditions
C) To uniquely reference each record
D) To include the appropriate subject information
2. Given the full data set SUBJECT.DEMO:

The following SAS program is submitted:
%macro MP_ONE(pname=report);
proc &pname data=SUBJECT.DEMO;
run;
%mend;
%MP_ONE(print)
%MP_ONE()
Which PROC step(s), if any, execute?
A) PROC REPORT and PROC PRINT
B) PROC REPORT only
C) No PROC steps execute
D) PROC PRINT only
3. What is the main focus of 21 CFR Part 11?
A) electronic submission requirements
B) statistical calculation requirements
C) trial protocol requirements
D) trial safety requirements
4. The following SAS program is submitted:

What is the value of the variable day when the data step completes?
A) 1
B) 8
C) 7
D) 6
5. Which statement correctly describes an aspect of a Phase II clinical trial?
A) designed to assess how well the drug works
B) in vitro and in vivo experiments using wide-ranging doses of the drug
C) designed to assess the pharmacovigilance, pharmacokinetics, and pharmacodynamics of a drug
D) randomized controlled multicenter trials on large patient groups
Solutions:
Question # 1 Answer: C | Question # 2 Answer: B | Question # 3 Answer: A | Question # 4 Answer: B | Question # 5 Answer: A |