Training: Development of the Informed Consent Form

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About course

 

This training is designed to help medical writing professionals effectively write Informed Consent Forms (ICFs) for participants taking part in clinical studies.

 

  • 1) understand the key terminology in the field of informed consent for participation in clinical studies,
  • 2) understand the regulatory basis for informed consent,
  • 3) know the required elements of an ICF and the source materials to use when writing an ICF, and
  • 4) be prepared for challenges and be aware of some general tips and tricks for writing an ICF.

 

Course:  Development of the Informed Consent Form

 

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Customer testimonial:

 

“Experienced and proactive medical writers. The writers exchange and update each other across documents and projects so that they use the latest processes, ways of working and company preferences. I’m impressed by their consistent quality and attention to detail.”

Associate Director Medical Writing