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Learning Practice

Public education edition | Version 2.4.0

For Clinical Research Associates Worldwide

FDA / ICH reference questions

Public reference material. Confirm current requirements and sponsor procedures before applying an answer.

Regulatory questions and source-based answers remain in English to preserve the wording of the reference library.

What are the CRA's responsibilities under ICH GCP 5.18.4?

What does 21 CFR Part 11 require for electronic signatures?

What is risk-based monitoring according to FDA guidance?

What essential documents are required before a trial begins?

What are the investigator qualification requirements?

What is the SAE reporting timeline under FDA regulations?

What are the requirements for source data under ICH GCP?

How should CRF corrections be handled per ICH GCP?

Educational reference material. Verify current requirements and sponsor procedures before use.

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