At Addmedica, only key and stategic functions are managed in house, notably Regulatory Affairs and Scientific, Medical and Marketing Expertise with experience of EU Centralized MA and US Approval, Named Patient and Early Access Program management and commercialization of an Orphan Drug throughout Europe and in the US. Addmedica is used to working with a network of high quality suppliers, Consultants and Partners for specific needs (i.e. labs research, manufacturing, clinical trials, medical affairs expertise, market access process, business development and licences…). If appropriate, Addmedica is also able to set up its own distribution structure in a territory including its own sales force in its areas of expertise (i.e. in France).
Addmedica’s main premises are located in Paris.