Subject or subject's representative is willing and able to provide written informed consent
Willing and able to give written informed consent.
Patient is able and willing to provide written informed consent
Be willing and able to provide written informed consent for the trial
Patient must be capable, willing, and able to provide written, informed consent
Willing and able to provide written informed consent.
Be willing and able to provide written informed consent for the trial
Willing and able to provide written informed consent
Be willing and able to provide written informed consent for the trial
Able and willing to provide written informed consent to participate in this study.
Willing and able to provide written informed consent for the study
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial
Willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial
Willing and able to give written, and dated, informed consent
Willing and able to provide written informed consent to participate in this investigational study.
Subject is willing and able to give prior written informed consent for investigation participation; and
Willing and able to give written informed consent
Willing and able to give written informed consent
Must be able and willing to give written informed consent.
Subjects must be willing to give written informed consent per institutional guidelines and must be able and willing to adhere to dose and visit schedules
Must be willing and able to provide written informed consent
Be willing and able to provide written informed consent for the trial
Willing and able to provide written informed consent
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial.
Be willing and able to provide written informed consent.
Be willing and able to provide written informed consent for the trial
Willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial
Patient must be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial
Must be willing and able to provide written informed consent
Be willing and able to provide written informed consent for the trial
Willing to provide informed written consent
Be willing and able to provide written informed consent for the trial
Willing and able to provide written informed consent.
Be willing and able to provide written informed consent for the trial
Willing and able to provide written informed consent
Willing and able to provide written informed consent for the trial
Is willing and able to provide written informed consent for the trial.
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial
Willing and able to provide written informed consent
Be willing and able to provide written informed consent for the trial
Willing and able to provide written informed consent
Willing and able to provide written informed consent
Must be willing and able to provide written informed consent
Be willing and able to provide written informed consent for the trial
Subjects must be willing to give written informed consent per institutional guidelines and must be able and willing to adhere to dose and visit schedules
Willing and able to provide written informed consent
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial
Willing and able to provide written informed consent
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for trial
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial.
Be willing and able to provide written informed consent for the trial
Is willing and able to provide written informed consent for the trial
Must be able and willing to give written informed consent
Be willing and able to provide written informed consent for the trial
Patient must be capable, willing, and able to provide written, informed consent
Willing and able to give written informed consent
Must be willing and able to provide written informed consent
Willing and able to give written informed consent
Willing and able to provide written informed consent.
Be willing and able to provide written informed consent
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial.
Must be able and willing to give written informed consent
Willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial
Willing and able to provide written informed consent for voluntary participation in the trial
Be willing and able to provide written informed consent for the trial
Be willing and able to provide written informed consent for the trial
Participant is willing and able to give written informed consent
Patient is willing and able to give written informed consent
Willing and able to provide written informed consent
Able and willing to provide written informed consent
Patient willing and able to provide written informed consent
Willing to provide written informed consent
Must be able and willing to give written informed consent
Able and willing to provide written informed consent to participate in the study
Patients must be able and willing to give written informed consent
Be willing and able to provide written informed consent
Be willing and able to provide written informed consent for the trial.
Be willing and able to provide written informed consent for the trial
Must be willing and able to provide written informed consent
Must be willing and able to provide written informed consent
Willing and able to give written informed consent.
Be willing and able to provide written informed consent for the trial
Willing and able to provide informed written consent
Able and willing to provide written informed consent
Be willing and able to provide written informed consent for the trial
Willing and able to give written informed consent
Patient must be capable, willing, and able to provide written, informed consent
Patient willing and able to provide written informed consent for the trial
Willing and able to provide written informed consent
Able and willing to provide written informed consent.
Willing and able to give written informed consent
Willing and able to give written informed consent
Willing and able to give written informed consent
Willing and able to provide written Informed Consent and adhere to study procedures.
Willing and able to provide written informed consent
Willing and able to give written informed consent
Willing and able to provide written informed consent.
Willing and able to provide written informed consent
Able and willing to give written informed consent.
4. Patient is able and willing to provide written informed consent to participate in the study.
Subject or subject's representative is willing and able to provide written informed consent
Subjects must be willing to give written informed consent and be able to adhere to dose and visit schedules.
Willing and able to provide written informed consent.
Willing and able to give written informed consent
Subject is willing to provide written informed consent
Able and willing to provide written consent
Willing to provide informed written consent
Willing and able to provide written informed consent
Patients must be willing and able to provide a written informed consent
Able and willing to provide written informed consent
Patients must be willing and able to provide written informed consent for the trial
Willing and able to provide written informed consent
Patient must be able and willing to provide written informed consent
Participant willing to provide a written informed consent
Willing and able to provide written informed consent
Subject must be able and willing to give written informed consent for a contrast enhanced ultrasound study of the prostate
Willing and able to provide informed written consent
Be willing and able to provide written informed consent for the trial
Willing and able to provide a written informed consent
Willing and able to provide written informed consent
Subjects are required to be willing and able to provide written informed consent
Be willing and able to provide written informed consent.
Patients must be able and willing to provide written informed consent prior to any study related procedure.
Be willing and able to provide written informed consent for the trial