As an associate of our Life Sciences practice, Marta Miglietti advises clients on European Union and national regulatory matters applicable to medicinal products. She assists clients in the different phases of marketing authorisation procedures and provides advice in addressing various issues in the context of promotional and marketing activities in the pharmaceutical sector.
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 regulatory framework governing data protection requirements in the pharmaceutical sector (e.g. informed consent templates). Marta also assists clients in the context of access to documents procedures.
Before joining Hogan Lovells in February 2016, 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 law, focusing on State aid; regulatory assistance; access to documents and data protection. She was admitted to the Brussels Bar (E-List) in March 2015.