Training: Development of the Informed Consent Form

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