Informed consent
A process in which a person learns key facts about a clinical trial, including potential risks and benefits, before deciding whether or not to participate in a study.
Informed consent continues throughout the trial
Medical disclaimer
The information on this page is for educational and informational purposes only and does not constitute medical advice in any way.
- It does not replace the advice of a physician, pharmacist or other healthcare professional.
- It does not represent a prescription of drugs, diagnostic exams or therapies.
- In case of symptoms, doubts or concerns about your health, always consult a qualified physician.
In case of emergency call 911 (US) or 112 (EU).