Alethios emphasizes compliance, ethical rigor, and participant protection. Many studies are approved by Internal Review Boards (IRBs) and some are built with regulatory procedures in place to make them suitable for agencies like the FDA. The platform includes built-in compliance tools, secure data handling, and transparency at every step.
Alethios makes every effort to ensure that you are always informed of the safety of study devices, interventions and other risks through the Consent process. That said, your safety also depends on honest and accurate reporting of your health status during enrollment. You’ll be asked to complete a screening process and sign an eConsent form that outlines any potential risks or requirements specific to a study, like allergies or intolerances to certain items. It’s important to read this carefully and share any relevant medical history so researchers can ensure the study is appropriate for you.
If you ever feel unsafe or that your health is in any way at risk, you may contact us using the support@alethios.com email address, phone number, or contact the investigator running your study (this will be available in your consent form). You may also use the Event Reporting tool to report a health or other event related to your well-being in the study. If you are ever in an emergency, immediately dial 911.