Written informed consent and authorization for release of personal health information obtained according to local laws.
Written authorization for use and release of health and research study information has been obtained.
Written authorization for use and release of health and research study information has been obtained
Signed informed consent form (ICF) providing agreement to adhere to the dosing schedule, report for all trial visits and authorization, use and release of health and research trial information
Signed informed consent form (ICF) providing agreement to adhere to the dosing schedule, report for all trial visits and authorization, use and release of health and research trial information
Signed and witnessed informed consent and signed authorization for the release of their protected health information
Able and willing to provide written authorization for use and release of health and research study information
Written informed consent and authorization for release of personal health information obtained according to local laws.
Provided written authorization for use and release of health and research study information.
Signed informed consent form (ICF) providing agreement to adhere to the dosing schedule, report for all trial visits and authorization, use and release of health and research trial information
Written authorization for use and release of health and research study information has been obtained
Participants must have agreed to and signed an authorization for the release of their protected health information
Written authorization for use and release of health and research study information (United States [US] sites only) has been obtained
Written Authorization for Use and Release of Health and Research Study Information (United States [US] sites only) has been obtained
Written Authorization for Use and Release of Health and Research Study Information has been obtained
Informed consent and authorization for the release of health information signed by the patient
Patients must have signed an authorization for the release of their protected health information.
Signed informed consent form (ICF) providing agreement to adhere to the dosing schedule, report for all trial visits and authorization, use and release of health and research trial information
Written authorization for use and release of health and research study information has been obtained
Written authorization for use and release of health and research study information has been obtained
Patients must sign study-specific informed consent and authorization for the release of their protected health information prior to registration; patients must be registered in the prior to treatment with study drug
Written authorization for use and release of health and research study information has been obtained
Patients must sign an authorization for the release of their protected health information
Able to provide written informed consent and authorization for release of health information
Signed HIPAA compliant research authorization (or equivalent for international sites) to release Personal Health Information to the SunCoast CCOP Research Base must be obtained prior to registration
Written authorization for use and release of health and research study information has been obtained
Written informed consent and authorization to use and disclose health information
Subject consent and authorization for the release of health information must be obtained according to local institutional guidelines
Patient must provide written authorization to allow the use and disclosure of their protected health information; NOTE: This may be obtained in either the study-specific informed consent or in a separate authorization form and must be obtained from the patient prior to study registration