The Israeli law states that all medical devices and diagnostics need to be registered with the Israel Ministry of Health (AMAR) in Israel before importation in order to protect the public from sub-standard products and ensure the safety and effectiveness of said products.
BioPlan’s team has expertise in this area of registration and management of the registration along with offering you the required printed matter support and evaluation.
We have the capability to register both “Professional Use” medical devices and diagnostics, as well with “General Population Use” products including updating the printed material in order to be completely compliant with all local requirements.; together with obtaining the Ministry of Health’s, Pharmacy Department’s product classification, if necessary. We will also expediate and coordinate the import licenses and “one-time” import licenses.