Emergo’s global medical device regulatory consulting division was established in 1997 to help U.S. medical device companies export to Europe. Emergo has grown to become a leading consultancy with more than 2,700 medical device and IVD clients worldwide. Today, they maintain offices
in 25 countries, offering a wide range of compliance and market access services. Among other things, they assist companies with global regulatory strategy, device registration, quality management system compliance, clinical trial consulting, in-country regulatory representation and distributor qualification.
visit website: emergogroup.com