Internship report on Blueclinical phase I unit

Bioavailability/Bioequivalence clinical trials are a promising area in Pharmaceutical R&D and it is very interesting being involved in this field. During the internship, I practiced assistance activities to Bioavailability/Bioequivalence clinical trials and this was my target for intervention wi...

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Detalhes bibliográficos
Autor principal: Moreira, Paula Cristina Leão (author)
Formato: masterThesis
Idioma:eng
Publicado em: 2018
Assuntos:
Texto completo:http://hdl.handle.net/10773/13413
País:Portugal
Oai:oai:ria.ua.pt:10773/13413
Descrição
Resumo:Bioavailability/Bioequivalence clinical trials are a promising area in Pharmaceutical R&D and it is very interesting being involved in this field. During the internship, I practiced assistance activities to Bioavailability/Bioequivalence clinical trials and this was my target for intervention within Blueclinical during ten months. During this time I also had opportunity to exercise nursing research activities due to my previous training in the area. This report aims to describe the activities in which I was involved, the learning points and the experience achieved about the conduction of Bioavailability/Bioequivalence clinical trials. During the internship I have developed clinical trial assistance activities and I learned a lot about the process of trial conduction, from the submission to the authorities to get their approvals until the process of reporting the results This job was a challenge and a continuous learning process. At the end of this period, I feel it was a rewarded effort and I would like to keep developing my skills in this area.