Sara Vidal Rivas is a pharmaceutical professional with extensive experience in Regulatory Affairs, Medical Affairs, and Clinical Development. She studied Pharmacy at Universidad Complutense de Madrid and later pursued a specialization in Regulatory Affairs at Pharmaceutical College of Madrid. Her journey in the pharmaceutical industry began with an internship at the European Medicines Agency (EMEA) where she gained experience in the Pharmacovigilance Sector. Over the years, she has worked for several renowned companies such as AbbVie and Janssen Pharmaceutical Companies of Johnson and Johnson, where she held various positions such as Medical Manager and Medical Affairs and Medical Education Manager. Sara has also worked for Genetrix, Cellerix S.A in Clinical Development and Regulatory Affairs roles. With her broad knowledge of regulations and laws governing the pharmaceutical industry, Sara has been instrumental in many drugs' clinical development and approval.