Signed, dated informed consent
Signed and dated informed consent
Ability to understand the purpose and risks of the study and provide 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
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.
Willing and able to give written, and dated, informed consent
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.
Ability to understand the purpose and risks of the study and provide signed and dated informed consent
Signed and dated written informed consent obtained from patient or legal representative.
Signed and dated informed consent
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
Signed and dated PICF obtained prior to initiation of any study-specific procedure and treatment.
Signed and dated written informed consent
Provide signed and dated informed consent prior to any study specific procedures.
Signed and dated written informed consent prior to admission to the study
Must be willing and able to participate and comply with all trial requirements and able to provide signed and dated informed consent prior to initiation of any trial procedures
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 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
Signed and dated informed consent.
Ability to understand the purpose of the study, provide signed and dated informed consent, and able to comply with all procedures
Patient provides signed and dated informed consent prior to initiation of any study procedures.
Provision of signed and dated, written informed consent
Signed and dated informed consent.
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
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;
Provide signed and dated informed consent form
The subject is able and willing to comply with study procedures and provide signed and dated informed consent
The subject is able and willing to comply with study procedures and provide signed and dated informed consent
The subject is able and willing to comply with study procedures and provide signed and dated informed consent
Provide signed and dated informed consent form.
The subject is able and willing to comply with study procedures and provide signed and dated informed consent
Voluntarily signed and dated written informed consent prior to any specific study procedure.
Voluntarily signed and dated informed consent
Written Informed Consent not obtained, signed and dated