Ability to provide signed Informed Consent Form
Be  years of age at the time the informed consent form is signed
Provide written informed consent prior to any study related procedure. (In the event that the patient is re-screened for study participation or a protocol amendment alters the care of an ongoing patient, a new informed consent form must be signed.)
Be  years old at the time the informed consent form is signed
Signed informed consent form
Patient or authorized proxy needs to have signed the informed consent form
Signed Informed consent form
Signed Informed Consent Form.
Subject has been informed of the study procedures and the treatment and has signed an informed consent form
Signed informed consent form in accordance with institutional policies prior to the initiation of high-dose therapy
Signed informed consent form must be obtained prior to any research procedure
Have signed the current approved informed consent form
Signed written informed consent form
Informed consent form signed by the subject
Signed informed consent form must be obtained prior to any study procedure
Signed Informed Consent Form
Signed informed consent form
Signed informed consent form
Signed informed consent form
Subjects provide signed written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
Signed informed consent form.
Patients must provide a signed informed consent form before any trial relates activities are carried out.
A signed informed consent form or minor assent form
A signed informed consent form or minor assent form
Signed informed consent form
Patient has provided a signed study informed consent form prior to performance of any study related procedure
The signed informed consent form prior to the performance of any study related procedures that are not considered part of standard of care
Signed informed consent form
Signed informed consent form
Patients who have not provided a signed informed consent form to participate in the study, obtained prior to the start of any protocol related activities.
Patients must give written informed consent; a copy of the signed informed consent form will be retained in the patients chart
Have signed an approved informed consent form for the study.
Signed Informed Consent Form
Signed Informed Consent Form
Signed Informed Consent Form
Signed Informed Consent Form
Patients must have a signed informed consent form prior to enrollment on study
Signed Informed Consent Form
Signed Informed Consent Form
Signed Informed Consent Form
Signed Informed Consent Form
The signed informed consent form
Signed informed consent form
(Patient participation) Signed written informed consent form
Signed informed consent form
Signed informed consent form from patient
Provide signed written informed consent, which includes compliance with the requirements and restrictions listed in the consent form.
Signed informed consent form
Subjects must have signed an approved consent form
Received and signed an informed consent form.
Signed informed consent form
Signed informed consent form.
Subjects must have received and signed an informed consent form.
Subjects must have received and signed an informed consent form.
Signed Informed Consent Form