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Regulatory and Clinical Consulting for the In-Vitro Diagnostics

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Regulatory and Clinical Consulting for the In-Vitro Diagnostics

By MARACA International

Regulatory and Clinical Consulting for the In-Vitro Diagnostics

By MARACA International
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MARACA International is your partner for CE-marking and US Food and Drug Administration (FDA) submissions, delivering excellent service.

It has a vision to improve lives through service excellence and a mission to provide best-in-class regulatory, quality and clinical services to medical device (MD) and in-vitro diagnostic device (IVD) manufacturers, clinical laboratories, pharmaceutical companies and notified bodies.

MARACA brings more than 20 years’ experience excellence for MD and IVDs.

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