Dor provides focused solutions specific to address regulatory requirements in the medical device industry. Services support Israeli companies that manufacture for local and international consumers, as well as importers to Israel. Dor works with all device classes (medical devices, active implantable medical devices and in vitro diagnostic medical devices), the United States (medical machine, contrivance, implant, in vitro reagent, or other similar or related article – Class I, II and III devices) and other countries.
Customers benefit from Dor’s device expertise and experience across the regulatory spectrum, for the following services:
Dor helps device manufacturers, importers, exporters and distributors obtain and maintain compliance, supporting the entire product lifecycle, from pre-market approval registration to maintenance of existing licenses.