MARACA International

Regulatory and Clinical Consulting for Medical Devices and In-Vitro Diagnostics

MARACA International provides regulatory and clinical consultation to support Conformité Européene (CE) and US Food and Drug Administration (FDA) applications for medical devices and in-vitro diagnostic devices (IVD).

MARACA International provides regulatory and clinical consultation to support Conformité Européene (CE) and US Food and Drug Administration (FDA) applications for medical devices and in-vitro diagnostics (IVD).

Based in Belgium, the company also offers medical, regulatory, and clinical affairs services to help medical device, IVD, and pharmaceutical firms get their medical devices to market quickly and effectively.