Sara Magalhães

Sara Magalhães works as Regulatory Affairs Consultant at Qdossier, a Celegence company. She provides regulatory affairs consultancy and services to both big- and small-sized pharmaceutical companies, covering a wide variety of products.

Sara holds a master in Pharmaceutical Sciences from the Faculty of Pharmacy of the University of Lisbon, Portugal. Working at Qdossier for 2 years, Sara first acted as a Regulatory Operations Associate, being part of data management and migration projects as well as publishing, compiling and submitting eCTD and NEEs dossiers. As Regulatory Affairs consultant, she provides, amongst other, procedural advice, guidance and document review for new marketing authorisation applications.

Sara’s areas of expertise are: regulatory affairs, market approval procedures, regulatory convergence & harmonization, data management regulatory initiatives and eCTD publishing and lean authoring.

  • Next: 14-15 Jun 2023 Live online

The FDA Drug Approval Process

Live online

A comprehensive overview of FDA procedures, requirements for marketing authorisations and recent developments affecting the drug approval process in the US

  • 12 CPD hours
  • Presented by Sara Magalhães