Willing and able to comply with scheduled visits, treatment schedule, laboratory tests and other requirements of the study.
Capable of giving signed informed consent, which includes compliance with requirements and restrictions listed in the informed consent form (ICF) and in the protocol
You may not be if
Pregnant or lactating woman
Any mental or medical condition that prevents the patient from giving informed consent or participating in the trial
Inability to perform regular electronic reporting
Clareo Health | Looking At Triple Negative Breast Cancer Patient Experience Patterns in Medical Trials
