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  4. Metodologias em Investigação Clínica:desenho de Protocolos, Recrutamento e Compliance

Metodologias em Investigação Clínica:desenho de Protocolos, Recrutamento e Compliance

Code 16708
Year 1
Semester L0
ECTS Credits 5
Workload OT(75H)/T(40H)/TP(20H)
Scientific area Health Sciences
Entry requirements Professionals with an interest in the development and implementation of Clinical Research Holders of a degree or higher in Health Sciences and related areas
Learning outcomes To provide students with an integrated and multidisciplinary view of Clinical Research and to offer them the tools and knowledge to carry it out with excellence in their areas of expertise.
To train highly specialized professionals to join research teams, in response to the urgent and necessary increase in Clinical Research in Portugal and the need for its quality.
Syllabus Clinical Research: historical context and current guidelines
Development, Management and Monitoring in Clinical Research
Methodologies in clinical research: protocol design, recruitment and compliance
Quality, monitoring, audits and inspections
Data processing and scientific communication
Main Bibliography Zgheib, N. K., Tomasic, S. L., & Branch, R. A. (2017, January 1). Chapter 15 - Good Clinical Practice and Good Laboratory Practice (D. Robertson & G. H. Williams, Eds.). ScienceDirect; Academic Press
Kandi, V., & Vadakedath, S. (2023). Clinical Trials and Clinical Research: A Comprehensive Review. Cureus, 15(2), 1–15.
Language Portuguese. Tutorial support is available in English.
Last updated on: 2024-08-02

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