Medical Device Registration and Approval Worldwide

Emergo Group has the expertise, resources and local presence to assist you in obtaining medical device and IVD registration in the largest and fastest-growing markets worldwide. Our offices across five continents can provide comprehensive support for medical device approval efforts wherever you seek to commercialize your product.

Medical device registration/approvals we can obtain on your behalf include:

We can help you obtain medical device approvals in more countries than any other consulting firm.

From our offices in the US, Canada, Mexico, Brazil, Germany, England, France, Russia, Israel, India, China, Japan, South Korea and Australia, Emergo Group consultants can provide deep expertise in the particular regulatory requirements of their respective medical device markets. Having locally based experts ready to assist you in your chosen markets—rather than remote consultants trying to manage medical device registration efforts from afar—can make a major difference in terms of an efficient and successful medical device approval for your product. In some markets, having a local presence is vital to effectively deal with complex regulatory environments.

More than 1,500 companies from 50 countries have trusted Emergo Group for medical device registration and approvals. Because Emergo Group maintains operations on a global scale, there is no need to hire multiple consultants to address specific market entry or regulatory issues during your medical device registration effort. Smaller consulting firms simply cannot provide the same breadth and depth of service as our combined institutional knowledge, field experience global presence we have built up through the sheer variety of manufacturers whose medical device approval processes we have supported.