ECM America MDD Notified Body Launches US Dedicated Website ECMamerica.com
ECM's dedicated website helps manufacturers understand evolving regulatory requirements and European Union CE Marking directives.
August 29, 2018 (FPRC) -- ECM (Ente Certificazione Macchine), a Medical Device Directive (MDD) Notified Body (#1282) and an accredited ISO 13485 Certification Body raises the level of support to help U.S. medical device manufactures bring their product to the European market. ECM helps manufacturers understand evolving regulatory requirements and EU CE Marking directives.
The launch of the dedicated website facilitates opportunities to help prepare U.S. companies for market entry success. The new website allows visitors to quickly navigate the site and find product and service information, resources, partners program, and valuable content to help support European market access. As a thought leader, the resource page will be regularly updated providing valuable content for manufacturers including authoritative white papers, recorded webinars, in-depth case studies, service information and the latest industry news. In addition, exclusive blog content captures industry trends and thought provoking content to help companies prepare for success.
Visitors are welcome to explore the website and sign up for ECM America’s newsletter at www.ecmamerica.com.
ECM (Ente Certificazione Macchine) is a Notified Body (#1282) and an accredited ISO 13485 Certification Body supporting European market access for medical devices and other products. Through offices, laboratories and an extensive partner network in Asia, North America, Europe, Middle East, ECM delivers reliable, efficient and responsive services. Learn how you can get your medical devices to market faster. Contact David Surber at david.s@ECMamerica.com or call 833-ECM-CERT (833-326-2378). Visit www.ECMamerica.com.
Send an email to Roy Strunin of https://ecmamerica.com/