Máster presencial
Barcelona
Duración : 1 Año
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Sedes
Localización
Fecha inicio
Objetivos
The objective of the program is to acquire the knowledge in scientific and regulatory, from early stage to late stage drug development, achieving the new approvals and applying an international market access strategy. The main areas and topics are related with the regulatory agencies FDA and EMA, emerging markets, price & reimbursement, management of drug approvals and government affairs.
A quién va dirigido
The program is design for MSc and PhD with and with a high interest in science, willing to develop their career out the laboratory and the bench, in different management positions along the pharmaceutical industry such as in regulatory affairs department, market access, health economics, or government affairs among others. The program is focus in acquiring a global perspective in how a new drug in developed from the laboratory to the patient and the stakeholders involved.
Requisitos
Bachelor degree or PhD in Lifesciences; Biotechnology, Biochemistry, Bioengineering, Pharmacy, Biologist, etc.
Temario completo de este curso