Frequently asked questions
Please do not hesitate to contact us if you have any other questions, if you want more information, or if you wish to receive our product lists.
How Does PanGenerika Work?
PanGenerika works with different models. Partners can choose dossiers from our extensive list of dossiers for licensing, choose dossiers from our extensive list of dossiers for sale, ask us to source dossiers from their wish list, or request other services in the business development or regulatory field.
How does the in-licensing process work?
If a partner shows interest in a product from our extensive list of dossiers for licensing, we will assist with the deal negotiations, dossier audit and registration of the product. After registration we can assist with the ordering process and go-to-market strategies. We always aim to get the best deal for our partners.
How does the dossier for sale process work?
If a partner shows interest in a dossier which we have for sale, we will request the index, overview, and synopsis of this dossier from our producer in order for the partner to carry out their due diligence on the dossier before they make the final decision on the sale.
Can PanGenerika assist with Regulatory Affairs?
Our regulatory affairs department screens the dossiers to make sure that the content and format meets all current regulations (GMP, NeeS-guidance, XML format, E-CTD). Naturally, our team will need the input and support of our partners for national requirements.