Issuance of registration certificates by ANVISA in the name of a distributor may limit your control over the device registration. The BRH will “own” not only the registration but also the GMP certification and only the BRH can grant permission for others to import using the approval in their name. Please note, once a BRH is assigned to the device, it cannot be transferred for commercial reasons (i.e. you wish to switch distributors) and can only be transferred, for example, if two companies merge or one is spun off the other. If you select us as the BRH, we will be identified on the registration and would fully cooperate with you so that you control the approval of your device and who can and cannot import your products.
In the event of recall and/or incident involving your medical device, especially one that occurs in the distribution system, will the distributor defend their company or yours?