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:

 

“I can really trust the Emtex writers to deliver a quality document on time, to reach out to me or team members when appropriate, and to adapt to our changes in process/template over time. The consistent quality of work– and that this is true of all the writers. The willingness and ability to learn and improve. The good balance between independent work and reaching out to me or the team when appropriate. The effective and friendly communication.”

Senior Medical Writing Leader