Signed written Institutional Review Board (IRB)-approved informed consent document
Ability to understand and provide signed informed consent that fulfills institutional review board (IRB)s guidelines
Signed informed consent approved by the Institutional Review Board
have read, understood and signed the informed consent form (ICF) approved by the Institutional Review Board (IRB);
Subjects must have signed and dated an Institutional Review Board (IRB)-approved written informed consent form in accordance with regulatory and institutional guidelines; this must be obtained before the performance of any protocol-related procedures that are not part of normal subject care
Voluntary signed and dated Institutional Review Board (IRB) approved informed consent form in accordance with regulatory and institutional guidelines
Written consent on an Institutional Review Board-approved informed consent form prior to any study-specific evaluation
Voluntary signed and dated Institutional Review Board (IRB) approved informed consent form in accordance with regulatory and institutional guidelines
Ability to understand and provide signed informed consent that fulfills Institutional Review Board (IRB) guidelines
Signed informed consent approved by the Institutional Review Board
Patients must have signed and dated an Institutional Review Board (IRB) approved written informed consent form in accordance with regulatory and institutional guidelines; this must be obtained before the performance of any protocol related procedures that are not part of normal subject care
Signed informed consent approved by the Institutional Review Board prior to patient entry
Signed informed consent approved by the Institutional Review Board prior to patient entry
Signed informed consent approved by the Institutional Review Board
Institutional Review Board (IRB)-approved informed consent obtained and signed
Patients must have signed informed consent both for this study and the research use of data in the UAB bone marrow transplantation (BMT) program's Institutional Review Board (IRB) registered clinical database
Signed, written Institutional Review Board (IRB)-approved informed consent form (ICF)
All patients must be informed about the study and have signed a current Institutional Review Board (IRB) approved informed consent
Subjects who voluntarily signed and dated Institutional Review Board approved informed consent form in accordance with regulatory and institutional guidelines. Hepatocellular Carcinoma Inclusion Criteria:
Ability to understand and provide signed informed consent that fulfills Institutional Review Board (IRB)s guidelines
Signed informed consent approved by the Institutional Review Board
Signed, Institutional Review Board (IRB)-approved written informed consent
Signed informed consent approved by the Institutional Review Board prior to patient entry
Signed informed consent approved by the Institutional Review Board prior to patient entry
Signed an Institutional Review Board (IRB)-approved informed consent document for this protocol
Signed an institutional review board (IRB)-approved informed consent document for this protocol
E . Absence of signed and dated Institutional Review Board (IRB)-approved participant informed consent form prior to enrollment into the study.
Signed, Institutional Review Board (IRB)-approved written informed consent
Signed, Institutional Review Board (IRB)-approved written informed consent
Ability to understand and provide signed informed consent approved by the Institutional Review Board prior to any study-related activities and within  days of first study dose
Signed and dated institutional review board (IRB)-approved informed consent before any protocol-specific screening procedures are performed.
Signed and dated Institutional Review Board (IRB)-approved consent form
Prospective study participants must be informed of the investigational nature of the study and must have signed an Institutional Review Board (IRB)-approved informed consent form in accordance with institutional and federal guidelines
Absence of signed and dated Institutional Review Board-approved patient informed consent from prior to enrollment in the study
Patients must have signed the current Institutional Review Board (IRB) approved informed consent prior to registration (see Informed Consent).
Institutional Review Board (IRB) approved, signed written informed consent
Signed, Institutional Review Board (IRB)-approved written informed consent
Institutional review board (IRB) approved signed written informed consent
Signed informed consent approved by the Duke Institutional Review Board
Signed informed consent approved by the Institutional Review Board prior to patient entry
Institutional Review Board (IRB) approved, signed written informed consent
Institutional Review Board (IRB) approved signed written informed consent
Signed Institutional Review Board (IRB) approved written informed consent
Subjects must have signed and dated an institutional review board (IRB) approved written informed consent in accordance with regulatory and institutional guidelines; this must be obtained before the performance of any protocol related procedures that are not part of normal subject care
Signed an Institutional Review Board (IRB)-approved informed consent
Signed written informed consent approved by the Institutional Review Board obtained prior to study entry
The study has been explained to the patient/volunteer and the subject has signed the Institutional Review Board (IRB)-approved informed consent form prior to optical measurements
Are able to give written informed consent in a manner approved by the Institutional Review Board and comply with the requirements of the study.
Patient must consent to be in the study and must have signed and dated an Institutional Review Board (IRB) approved consent form conforming to federal and institutional guidelines
Informed consent signed by participant, parent, or guardian according to the guidelines of the institutional review board
Have read and signed the Institutional Review Board (IRB)-approved informed consent form for participating in the study
PATIENT: Have read and signed the Institutional Review Board (IRB)-approved informed consent form for participating in the study
Written informed consent will be signed by the patients before the MRI based on the guidelines approved by the Ohio State University Institutional Review board
Informed consent signed by participant, parent, or guardian according to the guidelines of the institutional review board
INCLUSION CRITERIA FOR OPEN-ACCESS: Informed consent signed by participant, parent, or guardian according to the guidelines of the institutional review board
Signed, Institutional Review Board (IRB)-approved written informed consent
Institutional Review Board (IRB) written informed consent obtained and signed
Subjects must have signed Institutional Review Board (IRB)-approved informed consent documentation
Subjects must have signed an institutional review board (IRB)-approved informed consent document
Subjects (or their parent or legal guardian) must have signed Institutional Review Board (IRB)-approved assent/informed consent documentation