A00-281 Clinical Trials Programming Using SAS 9 Accelerated Version Exam – Tips

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SAS Institute A00-281 Exam Sample Questions

Question: 2

What is an international ethical and scientific quality standard for designing, conducting, recording and reporting trials that involve the participation of human subjects?

  1. 21 CFR Part 11
  2. Good Clinical Practices
  3. MedDRA
  4. WHODrug


Answer: B

Question: 2

What is an international ethical and scientific quality standard for designing, conducting, recording and reporting trials that involve the participation of human subjects?

  1. 21 CFR Part 11
  2. Good Clinical Practices
  3. MedDRA
  4. WHODrug


Answer: B

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Question: 2

What is an international ethical and scientific quality standard for designing, conducting, recording and reporting trials that involve the participation of human subjects?

  1. 21 CFR Part 11
  2. Good Clinical Practices
  3. MedDRA
  4. WHODrug


Answer: B

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Question: 4

A Statistical Analysis Plan describes a clinical trial as “A 12 week, double-blind, placebo-controlled, randomized, multi-center study.” Double-blind refers to which groups in this study?

  1. treatment and control group
  2. investigator and subjects
  3. statistician and sponsor
  4. sponsor and investigator


Answer: B

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Question: 2

What is an international ethical and scientific quality standard for designing, conducting, recording and reporting trials that involve the participation of human subjects?

  1. 21 CFR Part 11
  2. Good Clinical Practices
  3. MedDRA
  4. WHODrug


Answer: B

Question: 2

What is an international ethical and scientific quality standard for designing, conducting, recording and reporting trials that involve the participation of human subjects?

  1. 21 CFR Part 11
  2. Good Clinical Practices
  3. MedDRA
  4. WHODrug


Answer: B

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