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In today's global marketplace, the development and marketing of medical products is a highly regulated process with strict governmental requirements. Since 1980, Medical Device Consultants, Inc. (MDCI) has provided regulatory, clinical, and quality assurance consulting services to help medical device and diagnostic product manufacturers meet those requirements.
With locations in the United States and Europe, our professional staff has extensive FDA, industry, and healthcare experience and a thorough understanding of medical device development and testing, governmental approval processes, and compliance and quality assurance systems.
To ensure the highest quality service to our clients, our U.S. corporate office achieved ISO 9001 certification from BSI in 1998. This was upgraded to the ISO 9000:2000 standard in 2003.
We help manufacturers develop and implement cost-effective strategies and programs to meet the US FDA regulations and European requirements for their specific medical products and business objectives.
MDCI delivers custom solutions to a wide range of companies-- from start-up ventures to established multi-national corporations throughout the world.
Speak with a Consultant
Reach our Massachusetts office at 1-508-643-0434, Monday through Friday, 9:00 a.m. to 5:00 p.m. Eastern. Or click here and a consultant will contact you directly.
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