A clinical trial is a research study in human volunteers to determine the safety and efficacy of a new medicinal product. Pharmaceutical companies conduct clinical trials on their new products before they are approved by the government to market and sell their products.

Clinical trials offer safe medical treatment because the subjects are carefully supervised with physicians and nurses by way of several visits at a medical clinic. Clinical trials must be approved by the federal government and by an ethics committee before subjects receive the new products.

To qualify for a clinical trial, subjects are required to pass a medical examination conducted by a physician. The participation to clinical trials is voluntary. Subjects can withdraw at any time.

The information that is collected during clinical trials remains confidential. The identity of the subjects enrolled in clinical trials is not revealed to anyone.

Depending on the project, the clinical trials of Mediprobe Research may involve patients to treat an illness or healthy volunteer subjects.