MDCI: Medical Device Consultants, Inc.
Staff Bios & Product Experience CRO and Regulatory Consulting to the Medical DeviceCRO and Regulatory Consulting to the Medical Device CRO and Regulatory Consulting to the Medical Device and In Vitro Diagnostics Industries since 1980
For over 25 years, we’ve been helping manufacturers all over the world bring medical devices and in vitro diagnostic products to the marketplace with our innovative, cost-effective consulting services. With our extensive knowledge of applicable regulations, we’ve also made sure that clients remain in commercial distribution by maintaining post-marketing compliance.In short, our expertise can help you get your product successfully into the market-place and maintain compliance. Whether you’re just beginning the process, needto conduct a clinical trial, are about to undergo review by a regulatory body, orwish to ensure post-market compliance, MDCI is the one to call.
The Medical Device Regulatory Compliance Process

For more information, please click on your area of interest in the diagram to the left.

Current Issue:

What You Don't Know CAN Hurt You: FDA's New Approach to Postmarket Device Safety

Free guides, tips, and advice on how to effectively achieve and maintain compliance for your medical product
To speak with a consultant phone our U.S. office at 1-508-643-0434, or click here to have consultant contact you directly.
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