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Clinical Research Questions

Zen AI let’s you ask questions on the International Council for Harmonisation of Technical Requirements for Pharmaceuticals for Human Use Good Clinical Practice guideline – the ICH GCP E6(R3). Give it a shot!

Questions such as the following may be asked:

  • How does the informed consent process works?
  • How can I start a clinical trial?
  • Tell me more about it (continuing on any previous question)
  • What are the investigator obligations?

Please be patient, some questions take a few seconds to answer.

Disclaimer: the Zenbot chatbot or website do not pretend to recount accurately the ICH GCP E6 (R3) in any way. Zenbot may be prone to errors and the Zenbot project is at the stage of development. Zentrial AI is independent from the International Council for Harmonisation.