Signed, dated informed consent
Provision of signed and dated, written informed consent prior to any study specific procedures
Signed and dated informed consent
Written and voluntary informed consent understood, signed and dated.
Signed and dated written informed consent obtained prior to any study-specific evaluation.
Dated and signed IEC/IRB-approved informed consent.
Signed and dated written informed consent
Provision of signed and dated written informed consent prior to any study-specific procedures, sampling, and analyses. If a patient declines to participate in any voluntary exploratory research and/or genetic component of the study, there will be no penalty or loss of benefit to the patient and he/she will not be excluded from other aspects of the study.
Able to provide signed and dated informed consent before initiation of any study procedures.
Subject has signed and dated informed consent
Written and voluntary informed consent understood, signed and dated.
Patient must consent to the study and provide a signed and dated, written informed consent document prior to any study-specific procedures, sampling, or analyses.
Voluntarily signed and dated written informed consent prior to any specific-study procedure.
Patient has signed and dated informed consent
Signed and dated written informed consent.
Signed and dated written informed consent.
Signed and dated written informed consent obtained from patient or legal representative.
Signed and dated informed consent
Provision of signed and dated informed consent form (ICF).
Ability to provide a signed and dated consent or have a legally authorized representative to provide written and signed consent prior to the initiation of any research related procedures
Signed and dated written informed consent
Subject has signed and dated informed consent
Provision of signed and dated, written informed consent prior to any study specific procedures, sampling and analyses; including access to all archival tumour tissue (diagnostic and/or most recent samples)
Signed and dated PICF obtained prior to initiation of any study-specific procedure and treatment.
Signed and dated written informed consent
Provision of signed and dated, written Informed Consent Form (ICF) prior to any trial-specific procedures, sampling, or analyses. If a patient declines to participate in the voluntary pharmacogenetics component of the trial, he/she will not be excluded from other aspects of the trial.
Provide signed and dated informed consent prior to any study specific procedures.
Signed and dated written informed consent prior to admission to the study
Patients must have given written, signed and dated informed consent prior to registration on the study; NOTE: no study-specific screening procedures may be performed until consent has been given
A signed and dated written informed consent form is obtained from the subject
Signed and dated written informed consent
Signed and dated written informed consent
Signed and dated written ICF by the patient or legally acceptable representative prior to any study-specific procedures
Signed and dated informed consent of the patient, available before the start of any specific trial procedure.
Signed and dated informed consent document.
Informed consent document signed and dated by patient
Signed & dated informed consent prior to Screening evaluations
Must sign informed consent, witnessed, and dated prior to entry
Signed and dated written informed consent to participate in this clinical trial must be obtained prior to any study procedure
Provision of signed and dated, written informed consent prior to any study-specific procedures, sampling and analyses.
Signed and dated informed consent.
Patient provides signed and dated informed consent prior to initiation of any study procedures.
Provision of signed and dated, written informed consent
Provision of signed and dated written informed consent prior to any study specific procedures.
Signed and dated informed consent.
Provision of signed, written and dated informed consent prior to any study specific procedures
Provision of signed and dated, written informed consent prior to any study specific procedures, sampling and analyses
Provision of signed, written and dated informed consent prior to any study specific procedures
Signed and dated IRB/Approved Informed Consent
Able to provide signed and dated informed consent prior to initiation of any study procedures.
Signed and dated written informed consent prior to admission to the study
Subject has signed and dated informed consent
Signed & dated ICF prior to Screening evaluations
Patient must provide a signed and dated written informed consent prior to registration and any study-related procedures
PRE-REGISTRATION INCLUSION CRITERIA: Signed and dated informed consent document for study participation
Voluntarily signed and dated written informed consent
Voluntarily signed and dated written informed consent
Evidence of a personally signed and dated written informed consent to participate in the clinical study
Voluntarily signed and dated written informed consent
Signed and dated written informed consent
Written informed consent (IC) for trial participation must be signed and dated by the patient and the investigator prior to enrollment
Written consent to biological material submission, indicating the patient has been informed of and agrees to tissue and blood material use, transfer and handling, must be signed and dated by the patient and the investigator prior to any procedures specific for this trial
Signed and dated Informed Consent Form (by the patient or a legally acceptable representative as per the local regulations).
Signed and dated informed consent form (by the patient or a legally acceptable representative as per the local regulations) obtained prior to initiation of any study-specific procedure and treatment.
Provide signed and dated informed consent form
Written informed consent form signed and dated by the subject
Subject is capable of understanding and willing to provide a signed and dated written voluntary informed consent before any protocol specific procedures are performed
Signed and dated informed consent
Participant is able and willing to comply with study procedures, and signed and dated informed consent is obtained
Signed and dated written IRB approved informed consent;
Documented, signed, dated informed consent obtained prior to any study specific procedures being performed
Provide signed and dated informed consent form
Provide signed and dated informed consent form.
Patient, or the patient’s legally acceptable representative, must provide a signed and dated written informed consent prior to registration and any study-related procedures
Provision of signed and dated written informed consent prior to any study specific procedures, sampling analysis
Voluntarily signed and dated written informed consent prior to any specific study procedure.
Voluntarily signed and dated informed consent
Signed and dated informed consent document obtained prior to initiation of any study-specific procedure and treatment (by the subject or a legally acceptable representative as per the local regulations).
Written Informed Consent not obtained, signed and dated