i.dras GMBH

we are your partner for regulatory projects: development and marketing authorisation of human and veterinary medicinal products, certification of medical devices. regulatory consultancy is our core competence. we support you in all regulatory activities – from the early phases of the development of medical devices and medicinal products over the complete development phase and market access up to the marketing phase. the same applies to the "lateral entry" via in-licensing or out-licensing and/or the purchase and sale of products. we aim to reduce your daily workload and your project work. with our know-how we contribute to the successful and timely processing of your projects. the aim of the i.dras team is to always be up to date with regard to the regulatory requirements for human and veterinary medicinal products as well as for borderline medical devices. in this respect the focus does not only lie on the knowledge of relevant regulations purely in terms of content, but also on their