CibusMed’s scientific team can undertake or contribute as a contracted third-party the following:

• • • Designing and selecting the approval process of new products
    • Drafting, preparing and updating the approval files (in e-CTD format) which are submitted to the National, European and international Medicines Organizations
    • Evaluating the approval files in terms of their quality and completeness

Our team also conducts training seminars for industry sales representatives. The goals of these seminars include training of sales employees on how to best approach health providers and to transmit technical and scientific information, in an easily digestible format.