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SASInstitute Clinical Trials Programming Using SAS 9.4 Sample Questions:
1. The PROC COMPARE code below is intended to validate the results from a PROC FREQ.
Both the ProdFreqData and ValFreqData data sets contain 10 observations of the variable Frequency.
No other variables are present in these data sets.
proc compare base = ProdFreqData
comp = ValFreqData
out = FreqDiffs
outbase outcomp outdif outnoeq
method = exact
noprint;
run;
After successfully executing this PROC COMPARE step, what is a possible reason for the FreqDiffs file to contain 30 records?
A) The internal values of Frequency are different in the base and comparison data sets.
B) The variable types of Frequency are different in the base and comparison data sets.
C) The formatted values of Frequency are different in the base and comparison data sets.
D) The variable labels of Frequency are different in the base and comparison data sets.
2. The programmer runs a validation program of the SDTM DM domain which produces the following in the log in SAS:
What does the validator need to check?
A) The sort order of both the production and validation datasets.
B) The formatted data values for SEX and AGE.
C) The internal data values for SEX and AGE.
D) The labels of both the production and validation datasets.
3. Which validation technique involves two programmers writing separate programs to produce the same output, then comparing the result?
A) Peer Review
B) Independent Programming
C) Peer Matching
D) Identical Programming
4. Which OPTION displays all SAS language statements generated during macro execution?
A) MSTORED
B) MLOGIC
C) MPRINT
D) MRECALL
5. An action plan that describes what will be done in a drug study, how it will be conducted, and why each part of the study is necessary is called:
A) a clinical trial plan
B) a data management plan
C) a protocol
D) a statistical analysis plan
Solutions:
| Question # 1 Answer: A | Question # 2 Answer: C | Question # 3 Answer: B | Question # 4 Answer: C | Question # 5 Answer: C |





