It is a controlled study conducted by a group of research physicians on volunteers to verify the efficacy and safety of new medications, procedures, devices, or vaccines. It is supervised and approved by health authorities.

To verify if a new treatment is effective and safe, providing a new benefit compared to current knowledge.

Yes, most of our studies are between Phases 2 and 4—the final stages that measure the final efficacy or safety of a drug before it is marketed. An Independent Ethics Committee supervises patient safety and compliance with Good Clinical Practices, evaluates the design of each study, and protects participants' rights.

It means participating freely and voluntarily in a research study evaluating a new medication's safety or efficacy. The patient receives information about the trial and freely decides to participate. They have the autonomy to drop the study whenever they want. To participate, certain requirements must be met based on your medical condition.

We have over 100 research protocols in their final phases (3 and 4). All studies include next-generation medication and free medical care through a multidisciplinary team that looks after the participating patient’s well-being.