Internship report on Blueclinical phase I unit
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Tipo de documento: | Dissertação |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10773/13413 |
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. |
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Internship report on Blueclinical phase I unitBiomedicinaEnsaios clínicosIndústria farmacêuticaBioavailability/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.Ensaios clínicos de Biodisponibilidade/Bioequivalência são uma área promissora em I&D Farmacêutico, e é muito interessante estar envolvida neste âmbito. Durante o estágio pratiquei atividades de assistência a ensaios clínicos de Biodisponibilidade/Bioequivalência sendo este o meu alvo de intervenção na Blueclinical durante dez meses. Durante este tempo também tive oportunidade de exercer atividades de enfermagem de investigação devido à minha formação anterior na área. Este relatório tem como objetivo descrever as atividades em que estive envolvida, os pontos de aprendizagem e a experiência adquirida em relação à condução de ensaios clínicos de Biodisponibilidade/Bioequivalência. Durante o estágio desenvolvi atividades de assistência de ensaios clínicos e aprendi muito sobre o processo de condução do ensaio, desde a submissão do ensaio junto das autoridades para obter a sua autorização até ao processo de relatar os resultados. Este trabalho foi um desafio e um processo de aprendizagem contínua. No final desta etapa, sinto que foi um esforço recompensado e desejo continuar a desenvolver as minhas capacidades nesta área.Universidade de Aveiro2018-07-20T14:00:47Z2014-09-23T00:00:00Z2014-09-232016-09-23T14:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesisapplication/pdfhttp://hdl.handle.net/10773/13413TID:201588838engMoreira, Paula Cristina Leãoinfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-02-22T11:24:27Zoai:ria.ua.pt:10773/13413Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T02:49:17.888832Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse |
dc.title.none.fl_str_mv |
Internship report on Blueclinical phase I unit |
title |
Internship report on Blueclinical phase I unit |
spellingShingle |
Internship report on Blueclinical phase I unit Moreira, Paula Cristina Leão Biomedicina Ensaios clínicos Indústria farmacêutica |
title_short |
Internship report on Blueclinical phase I unit |
title_full |
Internship report on Blueclinical phase I unit |
title_fullStr |
Internship report on Blueclinical phase I unit |
title_full_unstemmed |
Internship report on Blueclinical phase I unit |
title_sort |
Internship report on Blueclinical phase I unit |
author |
Moreira, Paula Cristina Leão |
author_facet |
Moreira, Paula Cristina Leão |
author_role |
author |
dc.contributor.author.fl_str_mv |
Moreira, Paula Cristina Leão |
dc.subject.por.fl_str_mv |
Biomedicina Ensaios clínicos Indústria farmacêutica |
topic |
Biomedicina Ensaios clínicos Indústria farmacêutica |
description |
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. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-09-23T00:00:00Z 2014-09-23 2016-09-23T14:00:00Z 2018-07-20T14:00:47Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/masterThesis |
format |
masterThesis |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10773/13413 TID:201588838 |
url |
http://hdl.handle.net/10773/13413 |
identifier_str_mv |
TID:201588838 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.publisher.none.fl_str_mv |
Universidade de Aveiro |
publisher.none.fl_str_mv |
Universidade de Aveiro |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
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1799137543689601024 |