As an associate of the Brussels office, Marta advises clients on European Union and national regulatory matters in the pharmaceutical sector. She assists clients in the different phases of marketing authorisation procedures and provides advice in addressing various issues in the context of promotional activities of medicinal products.
Marta provides her advice in the development of clinical trials (e.g. drafting of clinical trial agreements) and she assists clients in relation to the laws and regulations governing data protection in the pharmaceutical sector (e.g. drafting informed consent templates). Marta also assists clients in the context of access to documents procedures.
Before joining Hogan Lovells, Marta worked as a trainee at the EU Affairs department of the Italian Chamber of Deputies and at the European Parliament (DG Presidency). She practiced in Italy and Brussels, gaining a practical understanding of the key aspects of the EU internal market laws, focusing on State aid; regulatory assistance; access to documents and data protection.