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:

 

“Expert writers with a thorough understanding of regulatory documents and requirements.
Customer oriented, on time delivery of documents, high quality at a reasonable price.
Ability to take on complex projects and deliver with outstanding quality.”

Director Medical Writing