If you represent a medical device company, please fill out the form below, select your area of interest, and we’ll get back to you to schedule free 30-min initial consultation.
We offer a wide range of services within the fields of Regulatoy Affairs (MDR/FDA), Quality Management and PRRC. We also offer Project Management and support you with implementing your Quality Management System.
We can offer assistance with your regulatory compliance in several regions throughout the world.
We can represent your company for this required position in order to maintain compliance to the EU MDR/IVDR.
We can help organizations meet customer, market and regulatory requirements.
We can serve as the US agent for medical device manufacturers who do not have a presence in the US.
CENIT Consulting,
Experienced Regulatory Affairs Advisors
Our mission is to guide our clients on their journey to success, with our professional support.
Kami is a founding partner and is heading up our EU region focusing on MDR/IVDR as well as our PRRC service.
Dan is a founding partner and is in charge of our US region focusing on US FDA regulations.
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