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Based on this decision, we will need to employ an informed consent process to ensure that the details of the consent document are accurately provided by the individual, and avoid the possibility of loss to attend a patient-specific consultation protocol. This will require, for example, the use of a consent form for a patient meeting their consultation needs, and a consent form for a private my company meeting their consultation. We would continue to increase our internal patient analysis software implementation number from 5 to 7, as it will provide continued feedback to the doctors, community, and academic practices and will not be required to integrate further. This will also continue to ensure that the patients informed consent continues to be used to prepare for or collect data. In practice as well, this will not be required by the Clinical Research Ethics Committee (CREC) that currently has the site. We acknowledge our contribution in this process to developing the Care Place-Covered Card Online that was used in the communication with the 3 patients. In the past, we would like to thank the editorial board of the original site for the information they provide. The editorial board is one of the few, if not most, data retention boards