Programa

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Study load
Compulsory subjects	Optional subjects	Internships in companies	Final Project Work	Total
20 ECTS Credits	0 ECTS Credits	30 ECTS Credits	10 ECTS Credits	60 ECTS Credits

Examen final: El examen final consistirá en la presentación final y entrega de la memoria (el proyecto fin de máster), además de las 5 presentaciones parciales que se realizarán a lo largo del máster. El tiempo máximo de exposición para la defensa del trabajo será de 20 minutos y habrá 10 minutos adicionales para preguntas y respuestas. (70%)
Otros: El tutor hará un Informe correspondiente de las PRÁCTICAS en las Empresas. (20%)
Asistencia: La asistencia será obligatoria (10%)

Compulsory subjects Academic course 2024/25
Subject	Languages	ECTS Credits	Type	Mode
Access to Clinical Trial Monitoring and Regulatory Affairs. Development of Competencies and Skills of Professionals [Transversal]. The R&D and Regulatory Ecosystem of the BioPharma and Healthcare Industry. Registration, Maintenance and Surveillance of Medicines and Medical Devices	Spanish	6	Obligatorio	Mixta
Development of Medicines and Medical Devices and its Involved Organizations. The Pharmacological Basis of Therapeutics. Design of a Clinical Trial. Statistics applied to Clinical Research	Spanish	4	Obligatorio	Mixta
The Start-up of a Clinical Trial. Ethical, Regulatory and Contractual Aspects of Clinical Trials. Monitoring, Quality Management and Closure of Clinical Trials	Spanish	7	Obligatorio	Mixta
Types of Clinical Trials. Clinical Trials in different Therapeutic Areas	Spanish	3	Obligatorio	Mixta
Internships in companies from 2024/25		30	Obligatorio

Compulsory subjects
Subject	Languages	ECTS Credits	Type	Mode
Research project from 2024/25	-	10	Obligatorio	-

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