SOCRA CCRP Practice Exam

Disable ads (and more) with a membership for a one time $2.99 payment

Study for the SOCRA CCRP Exam. Equip yourself with flashcards and multiple choice questions, each with hints and explanations. Boost your confidence for exam day!

Start Multiple Choice Practice Test
Start Flash Cards

Each practice test/flash card set has 50 randomly selected questions from a bank of over 500. You'll get a new set of questions each time!

Practice this question and more.

What FDA regulation governs the documents a sponsor should get from an investigator before trial initiation?

  1. 21 CFR 312.53(b)

  2. 21 CFR 312.53(c)

  3. 21 CFR 50

  4. 21 CFR 54

The correct answer is: 21 CFR 312.53(c)

Option A is incorrect because it pertains to the documents that the sponsor should get from the investigator after trial initiation, not before. Option C and D are incorrect because they refer to different regulations that are not specifically related to documents from investigators before trial initiation. The correct regulation is 21 CFR 312.53(b), which states that before a clinical trial begins, the sponsor must obtain a signed investigator statement and curriculum vitae from the principal investigator.

More Questions Like This