Informed consent

Definition:

A process where patients are given important information, including benefits and risks, about a procedure, test, or treatment to decide if they want to be treated, tested, or take part in a clinical trial.

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The digital patient pathway was co-developed by the European Society of Gynaecological Oncology (ESGO), the European Network of Gynaecological Cancer Advocacy Groups (ENGAGe), and AstraZeneca with funding provided by AstraZeneca.