CogniFit PRO

Cognitive Assessment Battery (CAB)® PRO

A collection of neuropsychological tests for health professionals and researchers. The assessment measures cognitive function and performs a complete cognitive screening, allowing users to quickly, conveniently, and accurately assess the well-being and cognitive profile of patients and research participants. Applicable via in-person consultation, in a laboratory setting, and remotely.

FDA Registration Number: 3017544020*.

CogniFit’s Cognitive Assessment Battery (CAB)® PRO is a leading professional tool that allows researchers, doctors, psychologists, and other health professionals to study in-depth the cognitive profile of children 7 years old and older, adolescents, adults, and seniors.

The application of this evaluation is simple and intuitive, ensuring that any professional can apply it without difficulty. In addition, it is designed so that it can be used both face-to-face in a consultation or laboratory setting, as well as remotely from the homes of patients or participants.

This neuropsychological test takes approximately 30-40 minutes to complete and is done entirely online. At the end of the evaluation, a complete results report with the user’s neurocognitive profile is automatically obtained. In addition, the assessment provides valuable information that, as professionals, can help us to detect if there is a risk of any disorder or other problem, to recognize its severity, and to identify the most appropriate support strategies for each case.

This neuropsychological assessment is recommended for professionals who want to know more about the brain function or cognitive, physical, psychological, or social well-being of the patient or participant. We recommend using this cognitive assessment as a supplement to a professional diagnosis, and never as a substitute for a clinical diagnosis.

Every CogniFit cognitive assessment is intended as an aid for assessing cognitive wellbeing of an individual. In a clinical setting, the CogniFit results (when interpreted by a qualified healthcare provider), may be used as an aid in determining whether further cognitive evaluation is needed.

If used for research purposes, all use of the product must be in compliance with appropriate human subjects' procedures as they exist within the researchers' institution and will be the researcher's obligation. All such human subject protections shall be under the provisions of all applicable sections of the Code of Federal Regulations.