Supervision and control of regulatory affairs. Responsible for the Regulatory Intelligence Core. Coordination of international regulatory affairs activities (registration/post-registration) of medicines and medical devices in America, Europe, Asia and Africa.

Registry and post-registry of medical devices. Control of company legal documentation (GMP). Inventory control of medical devices.

Technical-scientific support in activities related to patent evaluation, sanitary legalization of medicines, medical devices, food and cosmetics. Preparation of technical report for lawsuits involving the pharmaceutical area.

Preparation and submission of the DDCM and specific dossiers for each clinical trial. Technical evaluation of clinical research protocols and registration in national databases (Plataforma Brasil / Rebec). Support for monitoring clinical trials.