Medical Device Consultants, Inc. (MDCI) is a leading contract research organization providing consulting services to medical device and diagnostic product manufacturers and suppliers in the areas of:
- Regulatory Affairs
- Clinical Trials
- Quality Assurance and Compliance
- EU Authorized Representative
- CE Marking
With offices in the U.S. and Europe, MDCI is able to support your worldwide regulatory needs.
Our goal is to assist manufacturers in developing and implementing cost-effective regulatory and business strategies to meet U.S. FDA regulations, Canadian regulations, and European requirements for their specific medical products.
MDCI staff provides high-quality services to our clients in a timely and professional manner. As part of our corporate commitment to providing quality services, Medical Device Consultants, Inc. achieved ISO 9001 registration from the British Standards Institution (BSI) in 1998.