News
September 30, 2008
Medical Device Consultants, Inc. (MDCI) Launches New Website
Firm Assists Medical Device Manufacturers with FDA Regulatory Consulting and CRO Services
North Attleboro, MA September 30, 2008– Medical Device Consultants, Inc., (MDCI) a leading regulatory consulting firm and contract research organization (CRO) for the medical device industry, has launched a new website at http://www.mdci.com.
The new site provides a comprehensive overview of MDCI's consulting and CRO services to assist medical device manufacturers, including specific case studies that address a variety of medical device therapeutic areas, and helpful resources such as articles, whitepapers and other downloads.
"Bringing a new medical device to market in the U.S. and internationally can be a daunting process, especially for companies with limited experience working with the FDA or international regulatory bodies," said Lisa King, marketing manager at MDCI. "Our goal is to provide web visitors with useful, easy to find information about how to address the medical device regulatory and clinical trial challenges they may encounter as they navigate along the pathway from product concept to commercialization."
MDCI selected Backbone Media, Inc., (http://www.backbonemedia.com) an internet-marketing firm based in Waltham, Massachusetts as its partner for website redesign and enhancement. "Backbone was pleased to help MDCI provide a more valuable website experience", said Stephen Turcotte, president of Backbone Media, Inc. "We used an integrated online marketing communications approach, first improving site design and navigation and then employing a highly targeted SEO solution to make the site more accessible to medical device manufacturers who need help gaining FDA 510k clearance or PMA approval or conducting an effective medical device clinical trial."
About MDCI
MDCI (Medical Device Consultants, Inc.) is a full-service consulting firm and contract research organization (CRO) that helps emerging and established firms commercialize novel and innovative medical devices, in vitro diagnostics, and combination products.
MDCI helps clients conduct successful medical device clinical trials, achieve FDA and EU regulatory clearance and approval, and maintain compliance for medical device products in the U.S. and internationally. By leveraging our comprehensive knowledge of FDA and international regulations, clients capture and grow market share, increase productivity, and stay competitive in an increasingly complex global marketplace.
Contact Us
Reach our Massachusetts office at 1-508-643-0434, Monday through Friday, 9:00 a.m. to 5:00 p.m. Eastern. Or fill out our contact form and a consultant will contact you directly.