We out-license our registration dossiers, fully developed in house, for the partners to register and apply for a Marketing Authorisation in their country/-ies with their own trademark.
We are also willing to follow the registration procedure up to the granting of the Marketing Authorisation on behalf of our partner (in Europe) and then transfer the related MA once obtained directly to our partner.
In both cases, the partner becomes the MA holder and E-Pharma the finished product manufacturer.
We grant professional regulatory support from pre-approval to post-approval stage for the full lifecycle of the product.
Download our product pipeline to evaluate our available dossiers