Dissertations / Theses on the topic 'Medical and sanitary affairs'
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Godinho, Pedro Francisco Soares da Silva Mendes. "A closer look at medical affairs." Master's thesis, Universidade de Aveiro, 2014. http://hdl.handle.net/10773/13597.
Full textOver the last 10 years, the Pharmaceutical Industry has been under great scrutiny from regulators, healthcare professionals (HCPs) and patients in general, as in the past it was criticized for the use of aggressive sales and marketing tactics and unethical behaviour. To increase the transparency on the activities developed and its relationship with physicians, it has undergone significant changes in the way that it develops and markets medicines and medical devices. Many of these changes have led to an increase in the responsibility of Medical Affairs to inform the healthcare professionals’ community on the safe and appropriate use of the company´s medicines. Additionally, there is a trend to greatly limit physician access to traditional sales representatives who traditionally were industry’s vehicle of information and replace them by unbiased subject matter experts, the Medical Affairs colleagues. Much of this communication activity involves engaging and developing longterm relationships with key scientific opinion leaders in the disease area of interest. These scientific partnerships are crucial for the improvement of health outcomes that the pharmaceutical companies aim to achieve. The methods used by Medical Affairs to communicate the science vary from manuscripts in peer-reviewed journals, to congresses, continuous medical education meetings and discussion groups. More recently, digital channels have also been more frequently used to engage HCPs and even patients in this scientific exchange. Medical Affairs have significantly impacted the relationship with customers, continuing to build trust and value, transparency in all engagements, providing a balanced discussion of benefits and risks, and leveraging clinically robust dialogues on a peer-to-peer level. Medical Affairs activity, helping to address patients and physicians’ needs and promoting the appropriate use of medicines, will contribute to improve the reputation of the pharmaceutical industry.
No decurso dos últimos 10 anos, a Indústria Farmacêutica (IF) tem estado sob grande escrutínio por parte das Agências Regulamentares, profissionais de saúde e doentes no geral, sobretudo por ter sido criticada no passado pelas suas táticas de marketing e vendas agressivas e comportamento não ético. De forma a aumentar a transparência tanto das atividades desenvolvidas como da sua relação com os médicos, a Indústria alterou significativamente a forma como desenvolve e promove os medicamentos e dispositivos médicos. Muitas destas alterações levaram a uma maior responsabilização dos Assuntos Médicos (AM) na informação prestada à comunidade de prestadores de cuidados de saúde sobre o perfil de segurança e o uso apropriado dos medicamentos de uma empresa farmacêutica. Adicionalmente, verifica-se uma tendência para limitar significativamente o acesso dos delegados de informação médica aos prescritores, que tradicionalmente eram o veículo de informação da Indústria, substituindo-os por colegas imparciais especializados nos medicamentos (os colegas de Assuntos Médicos). Grande parte desta atividade informativa envolve estabelecer e desenvolver relações de longa duração com líderes de opinião numa determinada área terapêutica de interesse. Estas parcerias científicas são cruciais para a melhoria dos resultados em saúde que as companhias farmacêuticas pretendem alcançar. Os métodos utilizados pelos AM para comunicar ciência são diversos, abrangendo publicações em jornais com revisão por pares, congressos, sessões de educação médica contínua e grupos de discussão. Recentemente, os meios digitais passaram a ser também mais utilizados para envolver profissionais de saúde e doentes nesta partilha científica. Os AM impactaram significativamente o relacionamento com os clientes e continuam a construir uma relação de confiança e valor, de transparência, de discussão franca sobre benefícios e riscos e promovendo um diálogo clinicamente robusto entre pares. A atividade dos AM, que ajuda a colmatar as necessidades dos doentes e médicos e promove o uso correto dos medicamentos, contribuirá para melhorar a reputação da IF.
Sousa, Rui Eduardo Arantes de Passos. "4 years professional experience as a medical affairs manager." Master's thesis, Universidade de Aveiro, 2012. http://hdl.handle.net/10773/10877.
Full textNos últimos anos, os departamentos de Assuntos Médicos assumiram um importante papel estratégico nas companhias farmacêuticas e de biotecnologia. Em resposta a um aumento da regulamentação e de exigência de transparência, os departamentos de Assuntos Médicos mudaram o seu foco do apoio às atividades comerciais e de marketing para as responsabilidades na interface com os líderes de opinião, para o desenvolvimento médico, para as comunicações científicas e para outras tarefas médicas emergentes. Durante os quatro anos de experiência profissional como Gestor de Assuntos Médicos tive a oportunidade de desempenhar um conjunto alargado de tarefas que me permitiram desenvolver uma formação sólida, adquirindo ou reforçando competências fulcrais nesta área. Durante trinta e quatro meses trabalhei como Gestor de Assuntos Médicos para a área do Sistema Nervoso Central proporcionando um apoio mais direto às atividades de Marketing, Regulamentares e de Farmacovigilância. Nos últimos treze meses, após me ter tornado Gestor de Assuntos Médicos Internacional, assumi igualmente responsabilidades relacionadas com o desenvolvimento clínico de Fase IV, a gestão das comunicações científicas e escrita médica, a implementação de análises post-hoc e o apoio às atividades de Marketing global. Tive sempre como finalidade o alcançar da excelência no desempenho das tarefas sob minha responsabilidade, simultaneamente cumprindo os mais elevados padrões de ética e deontologia. Através do meu trabalho dedicado contribuí para o sucesso da minha companhia e, ao mesmo tempo, para a melhoria da saúde e do bem-estar de doentes e populações.
In recent years, medical affairs departments have taken on an important strategic role within pharmaceutical and biotechnology companies. In a response to the increased regulations and calls for transparency, medical affairs have shifted their focus away from commercial and marketing support to key opinion leaders interfacing responsibilities, medical advancement and medical communications activities as well as other emerging medical tasks. In my four years professional experience as a Medical Affairs Manager I have performed a wide variety of tasks that allowed me to develop a solid training, acquiring or strengthening core skills and competencies in this field. During thirty-four months I have worked as a Central Nervous System Medical Affairs Manager providing a more direct support to marketing, regulatory and pharmacovigilance activities. In the last thirteen months, after becoming International Medical Affairs Manager, I also took responsibilities related to phase IV clinical development, scientific communication management and medical writing, post-hoc analysis and global marketing support. I have always aimed at excellence while performing the activities under my responsibility, simultaneously attaining the highest professional and ethics standards. Through my devoted work I have positively contributed to the success of my company while contributing to the improvement of health and well-being of patients and populations.
Galindo, Elisabeth. "Description et évaluation d'une campagne d'information grand public sur la périnatalité dans le département de l'Hérault : "une naissance heureuse, c'est aussi votre affaire"." Montpellier 1, 1989. http://www.theses.fr/1989MON11195.
Full textTiveron, Daniela Verardino [UNESP]. "Inspeção pós-morte de bovinos: ocorrência de alterações sanitárias no abate e respectivo impacto em relação ao mercado globalizado." Universidade Estadual Paulista (UNESP), 2014. http://hdl.handle.net/11449/110620.
Full textA partir de 2005, a comissão do Codex Alimentarius deu início a uma nova empreitada no que diz respeito às práticas da inspeção ante e pós-morte, inserindo-as definitivamente nos planos de segurança e inocuidade. Recomenda-se, a adoção de métodos e técnicas de exames ou de análises que possuam enfoque ou características baseados no sistema APPCC (Análise de Perigos e Pontos Críticos de Controle – HACCP), que tem fundamentos científicos e caráter sistemático, permitindo identificar perigos específicos e medidas para seu controle - prevenção, redução ou eliminação, garantindo a inocuidade dos alimentos em margens de risco (Risk Analysis) aceitáveis internacionalmente. Este estudo visou à análise e a discussão das práticas vigentes durante a inspeção pós-morte de bovinos com base no monitoramento das ocorrências sanitárias durante o ano de 2012 e estudo retrospectivo da evolução dessas ocorrências entre os anos 2007 e 2011, com vistas à discussão e possível adequação dessas práticas com base nos requisitos e recomendações do Codex Alimentarius e do sistema de gestão de caráter preventivo definido pelo plano APPCC, focando-as em análises de risco. Nesse período, foram observados 17.981 casos de cisticercose (1,68%), 557 casos de linfadenite do tipo tuberculosa (0,05%), 1315 ocorrências de abscessos hepáticos (0,12%) e 235 casos de pneumonia (0,02%), num total de 1.067.584 animais abatidos. O índice geral para ocorrência de alterações sanitárias no exame pósmorte para o período foi de 1,9%, significando que dois em cada 100 animais abatidos demandam providências que salvaguardem a saúde dos consumidores. Embora pareça pequena, essa ainda é uma cifra muito elevada que impõe a necessidade do aprimoramento dos programas sanitários na exploração animal e sua efetiva adoção e responsabilização com base nas boas práticas de produção
Since 2005, the Codex Alimentarius committee began a new journey regarding the ante and post morten inspection practices, including this practice permanently at the security and safety plans. Methods and techniques tests adoption are recommended or analyze that have focus or characteristics based on HACCP program that have scientific fundamentals and systematic character that permit identify the specific hazard and measures for their control – prevention, reduction or elimination, ensuring the food safety in risk analysis international tolerable. This review aimed to analyze and discussion from adopted practices during the bovine post mortem inspection based on the sanitary occurrence monitoring during 2012, and based on retrospective study of these sanitary occurrences from 2007 to 2011, order to discuss and possible adequacy from these practices based on Codex Alimentarius requirements and recommendations. In this period were observed, 17.981 cases of cysticercosis (1,68%), 557 tuberculosis (0,5%), 13315 hepatic abscess (0,12%) and 235 pneumonia. (0,02%) in a total of 1.067.584 slaughtered animals. The general index to the sanitary changes occurrence at the post mortem exam at the period were 1,9%, what mean that each 100 animals slaughtered 2 need procedures to take care about customers heath safety. Although looks like a small quantity, it’s a big number that impose the necessity of the sanitary programs upgrading
Tiveron, Daniela Verardino. "Inspeção pós-morte de bovinos : ocorrência de alterações sanitárias no abate e respectivo impacto em relação ao mercado globalizado /." Jaboticabal, 2014. http://hdl.handle.net/11449/110620.
Full textBanca: Estevam Guilherme Lux Hoppe
Banca: Paulo Sérgio Jorge
Resumo: A partir de 2005, a comissão do Codex Alimentarius deu início a uma nova empreitada no que diz respeito às práticas da inspeção ante e pós-morte, inserindo-as definitivamente nos planos de segurança e inocuidade. Recomenda-se, a adoção de métodos e técnicas de exames ou de análises que possuam enfoque ou características baseados no sistema APPCC (Análise de Perigos e Pontos Críticos de Controle - HACCP), que tem fundamentos científicos e caráter sistemático, permitindo identificar perigos específicos e medidas para seu controle - prevenção, redução ou eliminação, garantindo a inocuidade dos alimentos em margens de risco (Risk Analysis) aceitáveis internacionalmente. Este estudo visou à análise e a discussão das práticas vigentes durante a inspeção pós-morte de bovinos com base no monitoramento das ocorrências sanitárias durante o ano de 2012 e estudo retrospectivo da evolução dessas ocorrências entre os anos 2007 e 2011, com vistas à discussão e possível adequação dessas práticas com base nos requisitos e recomendações do Codex Alimentarius e do sistema de gestão de caráter preventivo definido pelo plano APPCC, focando-as em análises de risco. Nesse período, foram observados 17.981 casos de cisticercose (1,68%), 557 casos de linfadenite do tipo tuberculosa (0,05%), 1315 ocorrências de abscessos hepáticos (0,12%) e 235 casos de pneumonia (0,02%), num total de 1.067.584 animais abatidos. O índice geral para ocorrência de alterações sanitárias no exame pósmorte para o período foi de 1,9%, significando que dois em cada 100 animais abatidos demandam providências que salvaguardem a saúde dos consumidores. Embora pareça pequena, essa ainda é uma cifra muito elevada que impõe a necessidade do aprimoramento dos programas sanitários na exploração animal e sua efetiva adoção e responsabilização com base nas boas práticas de produção
Abstract: Since 2005, the Codex Alimentarius committee began a new journey regarding the ante and post morten inspection practices, including this practice permanently at the security and safety plans. Methods and techniques tests adoption are recommended or analyze that have focus or characteristics based on HACCP program that have scientific fundamentals and systematic character that permit identify the specific hazard and measures for their control - prevention, reduction or elimination, ensuring the food safety in risk analysis international tolerable. This review aimed to analyze and discussion from adopted practices during the bovine post mortem inspection based on the sanitary occurrence monitoring during 2012, and based on retrospective study of these sanitary occurrences from 2007 to 2011, order to discuss and possible adequacy from these practices based on Codex Alimentarius requirements and recommendations. In this period were observed, 17.981 cases of cysticercosis (1,68%), 557 tuberculosis (0,5%), 13315 hepatic abscess (0,12%) and 235 pneumonia. (0,02%) in a total of 1.067.584 slaughtered animals. The general index to the sanitary changes occurrence at the post mortem exam at the period were 1,9%, what mean that each 100 animals slaughtered 2 need procedures to take care about customers heath safety. Although looks like a small quantity, it's a big number that impose the necessity of the sanitary programs upgrading
Mestre
Chang, Shelley. "Predicting Methicillin-Resistant Staphylococcus Aureus Carriage and Dissemination in a Veterans Affairs Medical Center." Case Western Reserve University School of Graduate Studies / OhioLINK, 2009. http://rave.ohiolink.edu/etdc/view?acc_num=case1238795542.
Full textSturdivant, Karen Diane. "Employee perceptions of the leadership style of the executive director of a medical center." DigitalCommons@Robert W. Woodruff Library, Atlanta University Center, 1988. http://digitalcommons.auctr.edu/dissertations/1586.
Full textBercaw, Edwin L. "A behavioral activation approach to smoking cessation for depressed smokers at veterans affairs medical centers." College Park, Md. : University of Maryland, 2007. http://hdl.handle.net/1903/7243.
Full textThesis research directed by: Psychology. Title from t.p. of PDF. Includes bibliographical references. Published by UMI Dissertation Services, Ann Arbor, Mich. Also available in paper.
Seago, Brenda. "UTILIZATION OF SIMULATION TO TEACH PELVIC EXAMINATION SKILLS TO MEDICAL STUDENTS: IMPLICATIONS FOR MEDICAL EDUCATION." VCU Scholars Compass, 2010. http://scholarscompass.vcu.edu/etd/2290.
Full textMoore, Scott C. "Anatomy of an Intervention: The History of a Change Effort in a Veterans Affairs Medical Center." University of Cincinnati / OhioLINK, 2007. http://rave.ohiolink.edu/etdc/view?acc_num=ucin1195592167.
Full textFormoso, Joseph. "Florida's medical malpractice tort reform a cognitive analysis of litigious, legislative promulgation and jurisprudence." Honors in the Major Thesis, University of Central Florida, 2012. http://digital.library.ucf.edu/cdm/ref/collection/ETH/id/553.
Full textB.A. and B.S.
Bachelors
Health and Public Affairs
Legal Studies
Zimmerman, Melissa M. "Leadership Practices of Supervisory Employees: An Exploration of Current Practices at a Southeastern Veterans Affairs Medical Center." Digital Commons @ East Tennessee State University, 2016. https://dc.etsu.edu/etd/3149.
Full textMontague, Diane M. "Medication errors in hospitals : to ERR is human, to report is divine." Honors in the Major Thesis, University of Central Florida, 2001. http://digital.library.ucf.edu/cdm/ref/collection/ETH/id/235.
Full textBachelors
Health and Public Affairs
Legal Studies
Grollmes, Deborah N. "Reduction of aberrant medical errors through United States Navy standardized militaristic training techniques in combination with technological innovations." Honors in the Major Thesis, University of Central Florida, 2001. http://digital.library.ucf.edu/cdm/ref/collection/ETH/id/224.
Full textBachelors
Health and Public Affairs
Health Services Administration
Mindemann, Lauren Nicole. "Exploring the Need for a Veteran-Specific Grief Program for the Robley Rex Veteran Affairs Medical Center (VAMC)." Miami University / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=miami1303397171.
Full textNoe, Colleen Marie. "Comparison of large group assistive listening devices in an adult classroom setting at the Veterans Affairs Medical Center /." The Ohio State University, 1994. http://rave.ohiolink.edu/etdc/view?acc_num=osu148785987993986.
Full textBellan, Natália. "Diretrizes para o processo de registro sanitário dos medicamentos." Universidade de São Paulo, 2013. http://www.teses.usp.br/teses/disponiveis/9/9139/tde-30072015-100420/.
Full textThe sanitary control in Brazil deserves a high level of consideration, because it is characterized by large social and economic importance. It encompasses a wide variety of products and services of various natures, as medicines, food, biological products, vaccines, blood products, sanitizing and disinfectants, toiletries, perfumes and cosmetics, control of ports, airports, frontiers stations and an extensive variety of health services. The National Agency for Sanitary Surveillance (ANVISA) was created in Brazil specifically as Article 3 of Law No. 9782/1999 and is relatively recent compared with regulatory agencies internationally, and has since evolved, gaining respect in the national and international level . Other regulatory agencies equally encompass important varieties of products and services similar from ANVISA. Even the Food and Drug Administration - (FDA) and European Medicines Agency (EMA) in its present \"rool\" medicine veterinarians, while in Brazil this type of product is regulated by the Ministry of Agriculture, Livestock and Supply (MAPA). The registration process in health monitoring system is a very valuable resource to ensure that commercialization of safe and effective products available to society. Any failure in the supply chain can impact on the quality criteria. Thus, the sanitary regulation on medicines covers the entire pharmaceutical chain since the early clinical research studies relating to the advertising standards. The objective of this work is to contribute in promoting knowledge of sanitary regulation for medicines by studying the organizational structure and responsibilities of ANVISA, and in parallel, perform analysis and comparison of the sanitary regulation between different categories of medicines, as well as discuss the regulatory strategy adopted by the pharmaceutical industry. As material of this research, we used essentially the national pharmaceutical the sanitary regulation, having as counterpoints the political and economic situation of the country, basing itself as a qualitative research method using the model document. With views to the organizational structure of drug regulatory agencies described in this study, it was found similarities inherent in the concepts and techniques regulatory, differentiating itself mainly by the fact that the Brazilian medicines for human and veterinary use are not covered under the responsibility of the same institution. Among the seven categories of drugs studied, the technical composition of their registration dossiers are considerably analogous, with different regulatory demands tangible to specific questions related to each type of medicine. In the analyzed period (2009 to 2010), in order to portray the regulatory trend adopted by the Brazilian pharmaceutical sector, the categories of generic medicines and similar are the ones that submitted more requests for deferrals and registries in the country.
Noblin, Alice M. "Intention to use a personal health record (PHR) a cross sectional view of the characteristics and opinions of patients of one internal medicine practice." Doctoral diss., University of Central Florida, 2010. http://digital.library.ucf.edu/cdm/ref/collection/ETD/id/4600.
Full textID: 028916585; System requirements: World Wide Web browser and PDF reader.; Mode of access: World Wide Web.; Thesis (Ph.D.)--University of Central Florida, 2010.; Includes bibliographical references (p. 160-172).
Ph.D.
Doctorate
Health and Public Affairs
Public Affairs
Schaefer, Jay M. "Is "good" good enough? a small area variation analysis of disparity in expressed rates of access to and satisfaction with child and adolescent healthcare services in east Central Florida." Doctoral diss., University of Central Florida, 2010. http://digital.library.ucf.edu/cdm/ref/collection/ETD/id/4603.
Full textID: 029050697; System requirements: World Wide Web browser and PDF reader.; Mode of access: World Wide Web.; Thesis (Ph.D.)--University of Central Florida, 2010.; Includes bibliographical references (p. 117-123).
Ph.D.
Doctorate
Health and Public Affairs
Public Affairs
Teeple, Lisa J. "Historical development of selected design amenities in central Indiana rural school buildings, 1875-1915." Virtual Press, 1993. http://liblink.bsu.edu/uhtbin/catkey/865947.
Full textDepartment of Architecture
Perez, Bianca. "A root cause analysis of the barriers to transparency among physicians a systemic perspective." Doctoral diss., University of Central Florida, 2011. http://digital.library.ucf.edu/cdm/ref/collection/ETD/id/4821.
Full textID: 030646191; System requirements: World Wide Web browser and PDF reader.; Mode of access: World Wide Web.; Thesis (Ph.D.)--University of Central Florida, 2011.; Includes bibliographical references (p. 126-142).
Ph.D.
Doctorate
Health and Public Affairs
Public Affairs
Pereira, Carla Raquel Xavier. "The evolving profile, role and relevance of the medical director in a pharmaceutical company." Master's thesis, Universidade de Aveiro, 2015. http://hdl.handle.net/10773/15616.
Full textOver the last years, operations in Pharmaceutical Companies have become more complex, trying to adapt to new demands of the market environment. Overall, the observed change of paradigm requires adapting, mainly by the setting of new priorities, diversification of investments, cost containment strategies, exploring new markets and developping new sets of skills. In this context, new functions have been created, the relevance of some has diminished, and the importance of others has arisen. Amongst these, the medical structure within a Pharmaceutical Company, increased to meet demands, with companies adopting different models to respond to these needs, and becoming a pillar to the business. Assuming the leading role within a medical department, the medical director function often lies in the shadow. It is a key function within Pharma Industry, either on a country or on a Global basis. It has evolved and changed in the past years to meet the constant demands of a changing environment. The Medical Director is a highly skilled and differeniated professional who provides medical and scientific governance within a Pharmaceutical company, since early stages of drug development and up to loss of exclusivity, not only but also by leading a team of other physicians, pharmacists or life scientists whose functions comprise specificities that the medical director needs to understand, provide input to, oversee and lead. As the organization of Pharmaceutical Companies tends to be different, in accordance to values, culture, markets and strategies, the scope of activities of a Medical Director can be broader or may be limited, depending on size of the organization and governance model, but they must fulfil a large set of requirements in order to leverage impact on internal and internal customers. Key technical competencies for medical directors such as an MD degree, a strong clinical foundation, knowledge of drug development, project and team management experience and written and verbal skills are relatively easy to define, but underlying behavioural competencies are more difficult to ascertain, and these are more often the true predictors of success in the role. Beyond seamless proficiency in technical skills, at this level interpersonal skills become far more important, as they are the driver and the distinctive factor between a good and an excelent medical director. And this has impact in the business and in the people doing it.
Nos últimos anos, as operações das empresas farmacêuticas têm-se tornado mais complexas, tentando adaptar-se às novas exigências do ambiente de mercado. Globalmente, a mudança de paradigma observada requer adaptação, principalmente através do estabelecimento de novas prioridades, diversificação dos investimentos, estratégias de contenção de custos, explorando novos mercados e desenvolvendo novos conjuntos de competências. Neste contexto, novas funções foram criadas, a importância de algumas diminuiu, e a importância de outras emergiu. Entre estas, a estrutura médica dentro de uma empresa farmacêutica aumentou para responder às exigências, com as empresas a adoptarem diferentes modelos para responder a estas necessidades, tornando-se um pilar para o negócio. Assumindo o papel de lider dentro de um departamento médico, a função de diretor médico permanece muitas vezes na sombra. É uma função chave dentro da Indústria Farmacêutica, seja num país ou numa base global. Esta função tem evoluído e mudado nos últimos anos para responder às exigências constantes de um ambiente em mudança. O Diretor Médico é um profissional altamente qualificado e diferenciado que confere orientação médica e científica dentro de uma empresa farmacêutica, desde as fases iniciais de desenvolvimento de medicamentos e até perda de exclusividade, não só mas também por liderar uma equipa de outros médicos, farmacêuticos ou cientistas, cujas funções incluem especificidades que o diretor médico precisa compreender, contribuir para, supervisionar e liderar. Como a organização das empresas farmacêuticas tende a ser diferente, de acordo com os valores, cultura, mercados e estratégias, o âmbito das actividades de um diretor médico pode ser mais amplo ou pode ser limitado, dependendo do tamanho e do modelo de organização e governança, mas deve cumprir um largo conjunto de requisitos a fim de maximizar o seu impacto sobre os clientes internos e externos. Competências técnicas fundamentais para diretores médicos, como uma especialização em Medicina, uma forte base clínica, conhecimento de desenvolvimento de medicamentos, experiência em gestão de equipas e de projectos, e elevada capacidade escrita e verbal são relativamente fáceis de definir, mas competências comportamentais subjacentes são mais difíceis de encontrar, e estas são mais frequentemente os verdadeiros preditores de sucesso na função. Além da proficiência irrepreensível em habilidades técnicas, a este nível as habilidades interpessoais tornam-se muito mais importantes, pois são o condutor e o factor distintivo entre um bom e um excelente diretor médico. E isso tem impacto no negócio e nas pessoas que nele trabalham.
Duffy, Brianne Michelle. "Identification of stressors related to emergency department employment." Honors in the Major Thesis, University of Central Florida, 2003. http://digital.library.ucf.edu/cdm/ref/collection/ETH/id/315.
Full textBachelors
Health and Public Affairs
Nursing
Opper, Scott. "Redesigning the American healthcare system." Honors in the Major Thesis, University of Central Florida, 2000. http://digital.library.ucf.edu/cdm/ref/collection/ETH/id/400.
Full textBachelors
Health and Public Affairs
Social Work
Sookdeo, Suzette S. "The Relationship Between the Utilization of Student Support Services and Overall Satisfaction in Medical School." Scholar Commons, 2016. http://scholarcommons.usf.edu/etd/6588.
Full textHubbard, Laura. "Factors Related to Adult Violence and Aggression in Healthcare Settings." Honors in the Major Thesis, University of Central Florida, 2004. http://digital.library.ucf.edu/cdm/ref/collection/ETH/id/420.
Full textBachelors
Health and Public Affairs
Nursing
Rehnström, Ida. "MedTech Firms' Business Model Alignment with Healthcare Institutional Logic : Successful Commercialization." Thesis, Luleå tekniska universitet, Institutionen för ekonomi, teknik och samhälle, 2021. http://urn.kb.se/resolve?urn=urn:nbn:se:ltu:diva-85334.
Full textAugusto, Ana Isabel Santos. "Curricular internship in a clinical pharmacology unit." Master's thesis, Universidade de Aveiro, 2015. http://hdl.handle.net/10773/14882.
Full textThe present internship report is a detailed description of my experience in the curricular internship performed at the Clinical Pharmacology Unit of the Instituto de Medicina Molecular, from October 13th 2014 to June 5th 2015. This internship was performed as part of the second and final year of the Master’s Degree in Pharmaceutical Biomedicine of the University of Aveiro. During the course of the experience I had the opportunity to participate in several projects in collaboration with different teams, most relevantly the activities related to the regulatory submission of a clinical trial in Portugal and related to the training in Pharmacovigilance. This internship has allowed me to put into practice the knowledge acquired during my academic training and deepen my knowledge on Clinical Research in a practical perspective. Additionally, it has also allowed me to improve many of skills and to understand my interests, capacities, weaknesses and strengths. In conclusion, I can affirm that this internship was an outstanding training and a very valuable professional and personal experience, for the main established objectives were achieved and exceeded.
O presente relatório de estágio descreve detalhadamente a minha experiência no estágio curricular realizado na Unidade de Farmacologia Clínica do Instituto de Medicina Molecular, desde 13 de Outubro de 2014 até 5 de Junho de 2015. Este estágio foi realizado como parte do segundo ano do Mestrado em Biomedicina Farmacêutica da Universidade de Aveiro. Durante o decorrer desta experiência, tive a oportunidade de participar em diversos projetos em colaboração com diferentes equipas, destacando-se as atividades relacionadas com a submissão de um ensaio clínico em Portugal e as atividades no âmbito da formação em Farmacovigilância. Este estágio possibilitou-me pôr em prática os conhecimentos obtidos durante a minha formação académica e aprofundar o meu conhecimento sobre investigação clínica, numa perspetiva prática. Para além disso, permitiu-me melhorar as minhas competências e perceber os meus interesses, capacidades, pontos fracos e fortes. Concluindo, posso afirmar que este estágio foi uma aprendizagem excelente e uma experiência de grande valor a nível profissional e pessoal, tendo conseguido atingir e ultrapassar os principais objetivos estabelecidos.
Binnie, Phillip B. "The effect of spirituality class on improving spiritual assessment scores and the relationship of spiritual assessment scores to length of stay of patients admitted to the psychiatric residential rehabilitation treatment program at the Miami Veterans Affairs Medical Center." Theological Research Exchange Network (TREN), 1997. http://www.tren.com.
Full textEsquivel-Yániz, Sonia Hildelisa. "Seguridad de equipos electromédicos: regulación sanitaria para la protección de la salud." Tese apresentada ao Programa de pós-graduação em Saúde Coletiva, 2011. http://www.repositorio.ufba.br/ri/handle/ri/10917.
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Trata-se de um estudo cujo objeto é a regulação sanitária de equipamentos eletromédicos, entendida como o controle sanitário desenvolvido pelo Estado, por meio das ações de vigilância sanitária, visando o controle de riscos e a segurança desses equipamentos. Tem como objetivo descrever e analisar o sistema regulatório brasileiro desses equipamentos a partir das instituições que o compõem, seus instrumentos e processos no exercício do controle sanitário, nos diferentes momentos regulatórios. Trata-se de um estudo de caso, tipo exploratório, tendo-se tomado como traçadores dois equipamentos eletromédicos: o ventilador pulmonar e o mamógrafo. Para a produção de dados foram utilizadas as técnicas de análise documental, entrevistas semi-estruturadas com informantes-chave e observação direta que permitiram descrever as bases normativas, os instrumentos e processos de controle sanitários aplicados ao longo do ciclo de vida dos equipamentos, pelos órgãos de vigilância sanitária e outras entidades que participam do controle. Também foram registradas considerações de fabricantes e usuários sobre as ações de controle sanitário e as limitações em sua execução. Os dados foram classificados e ordenados em uma matriz construída a partir do marco referencial do estudo e das categorias analíticas e operacionais definidas. Os resultados descrevem e analisam os componentes do processo regulatório brasileiro dos equipamentos eletromédicos, as instituições que compõem o sistema regulatório, seus instrumentos, processos e práticas, dificuldades e limites no exercício da regulação sanitária, nos diferentes momentos, bem como caracteriza a relação entre o sistema brasileiro e as normativas recomendadas por organizações internacionais. Foram evidenciadas dificuldades no exercício da regulação sanitária desses produtos, em face da dependência científica e tecnológica do Brasil, dos estágios iniciais dessa atividade no país e a pouca expertise dos profissionais de vigilância sanitária e de outras instituições reguladoras no relativo ao controle de riscos.
Salvador
Stalling, Veda. "The Phenomenological Evaluation of Social Worker Competencies in Patient-Centered Medical Homes." ScholarWorks, 2016. http://scholarworks.waldenu.edu/dissertations/1871.
Full textRibeiro, Eduardo Manuel Fernandes da Silva. "O médico na indústria farmacêutica: contributo para o enquadramento da atividade." Master's thesis, Universidade de Aveiro, 2015. http://hdl.handle.net/10773/15789.
Full textAo longo desta dissertação de mestrado pretendemos analisar e discutir o papel do Médico na Indústria Farmacêutica, contribuindo para um melhor enquadramento de uma atividade ainda não muito conhecida. A partir da análise da implementação da Indústria Farmacêutica em Portugal, descrevemos o seu contributo para a Sociedade aliado ao valor do medicamento. Descrevemos a Medicina Farmacêutica, o treino da atividade e alguns dos órgãos relevantes nesta área, como a Competência em Medicina Farmacêutica da Ordem dos Médicos e a Associação dos Médicos Portugueses da Indústria Farmacêutica. De uma forma detalhada caraterizamos as atividades e competências do Médico nesta indústria que reforçamos com uma análise de um questionário efetuado com as opiniões de colegas Portugueses e estrangeiros com experiência nesta área do conhecimento. Concluímos, reconhecendo a importância da atividade, da sua caraterização e dos seus desafios futuros.
Throughout this master thesis we intend to analyse and discuss the role of the Physician in the pharmaceutical industry, contributing to a better framework of a not widely known activity. From the analysis of Pharmaceutical Industry implementation in Portugal, we describe their contribution to Society, together with the value of the drug. We describe the Pharmaceutical Medicine, the training activity and some of the relevant bodies in this area, such as the Competence in Pharmaceutical Medicine from the Portuguese Medical Association and the Association of Portuguese Physicians from Pharmaceutical Industry. We did a detailed characterization of the competencies and responsibilities of the Physician at this industry that was reinforced with an analysis of a questionnaire carried out with the views of Portuguese and foreign colleagues with experience in this area of knowledge. We conclude, recognizing the importance of the activity, its characteristics and its future challenges.
Bellan, Natália. "Diretrizes regulatórias aplicáveis à cadeia dos produtos para saúde." Universidade de São Paulo, 2016. http://www.teses.usp.br/teses/disponiveis/9/9139/tde-20062016-153219/.
Full textThe science and technology increasingly been providing advancements in innovative products. Particularly in the health score is eminent synergism between the materials used, their properties of biocompatibility, biofunctionality, processability, sterility and applicability area of the human body. The pharmaceutical sector to present great complexity requires multidisciplinary knowledge, up to date and in line with international trends. The National Health Surveillance Agency (ANVISA) has under its responsibility extensive range of goods, services and products, among them are correlates, which also includes medical devices. Medical devices are classified according to their risk in Brazil may present up to four classes, and classes III and IV which characterize the greatest risk. For some products, because of their health risk, it is compulsory Compliance Certification by the National Institute of Metrology, Quality and Technology (INMETRO) prior to granting its sanitary registry by ANVISA. From among the technical standards the INMETRO are the standards of the Brazilian Association of Technical Standards (ABNT) and in his absence, the standards of the International Organization for Standardization (ISO).Other technical and regulatory requirements must be included for the purpose of proving the safety and efficacy of products. However, the sanitary regulations inherent in this product category is still incipient in the country. The resourcefulness of the productive sector in this segment can be evidenced by the increase in new requests in ANVISA and its growth in the trade balance. However, there is little study and understanding of the regulated and regulatory sector concerning the mutual relationship between ANVISA, INMETRO and ABNT and on the sanitary regulation applicable to obtaining the approval of the product for consumption. In the context of the demands indicated the objective of this study was to evaluate the regulatory procedure applicable to the production chain of medical devices in order to understand the relationship between ANVISA, INMETRO and ABNT in ensuring quality, safety and efficacy of products. The methodology used in this study was the qualitative research. With the assistance of documentary research it was found that the Brazilian regulatory process is complex, specific and robust and has similar structure and requirements of the United States and European Union. The postmarketing monitoring is an international trend and ANVISA has adopted often aiming to monitor the quality of marketed products. The three institutions have defined and regulated competences and interrelation through advisory boards mechanisms. The case study characterized the profile of professionals in the regulated sector has a large percentage of training in health and post-graduate level, but the level of knowledge of the main concepts related to medical devices is partial, reinforcing the need for incentives training of human resources in health regulation.
Fagelson, Marc A., and Richard H. Wilson. "Integrating University and VAMC Resources: Development of an AuD Program." Digital Commons @ East Tennessee State University, 2004. https://dc.etsu.edu/etsu-works/1613.
Full textZhang, Lei. "Uncompensated Care Provision and the Economic Behavior of Hospitals: the Influence of the Regulatory Environment." Diss., unrestricted, 2008. http://etd.gsu.edu/theses/available/etd-02242009-152847/.
Full textTitle from file title page. Paul G. Farnham, committee chair; Patricia G. Ketsche , Douglas S. Noonan (Ga. Tech.), Shiferaw Gurmu, Karen J. Minyard, William S. Custer, committee members. Description based on contents viewed June 11, 2009. Includes bibliographical references (p. 146-153).
Muñoz, Susana Inés Segura. ""Impacto ambiental na área do aterro sanitário e incinerador de resíduos sólidos de Ribeirão Preto, SP: avaliação dos níveis de metais pesados"." Universidade de São Paulo, 2002. http://www.teses.usp.br/teses/disponiveis/22/22133/tde-25072003-084308/.
Full textSolid waste may content toxic chemical substances such as heavy metals that are present in materials generated by industries, agricultural activities, laboratories, hospitals and houses. The contamination with heavy metals has a wide spectrum of toxicity that includes neurotoxic, hepatotoxic, nephrotoxic, teratogenic, carcinogenic or mutagenic effects. Since 1989, a municipal landfill site (MLS) for urban waste disposal has been in operation in Ribeirao Preto (Sao Paulo, Brazil) integrated with a medical waste incinerator plant (MWIP). This study aimed to do a diagnostic of the heavy metal levels in MLS and MWIP area, in 2000 and 2001. The total cadmiun (Cd), chromium (Cr), lead (Pb), manganese (Mn), zinc (Zn), cooper (Cu) and mercury (Hg) levels were analysed by Atomic Absortion Spectrophotometry in soil, water, percolated liquid and vegetables, in previously delimitated points. Samples from Santa Teresa Forest Ecological Station of Ribeirao Preto were collected as control samples. The results showed that, in general terms, the heavy metals detected in soil and vegetal samples in that area showed significant higher concentrations when compared with Santa Teresa Forest samples. The highest concentrations were detected to the North direction, these results can be associated with the topographic gradient in the area, the prevailing winds and the Incinerator localization. Special atention should be given to Cd, Mn and Cu levels detected in soil samples, that showed higher concentrations that those recomended for agricultural soil in Sao Paulo State by the Environmental Sanitation Company (CETESB). The percolated liquid also showed Cd, Pb, Mn and Cu levels higher than the maximum recomended levels according to the Sao Paulo State Law (Decreto 8486/76). The water samples showed levels according to the Brasilian Health Ministry Law (Portaria 1469/2000). Taking into account that few researches had been developed on this thematic in Brasil, the obtained results constituted an instrument for the decision makers and public managers, not only for Ribeirao Preto and region but for other cities around the country.
Slade, Catherine Putnam. "Does Patient-Centered Care affect Racial Disparities in Health?" Digital Archive @ GSU, 2007. http://digitalarchive.gsu.edu/pmap_diss/24.
Full textЯременко, Людмила Миколаївна, Людмила Николаевна Яременко, Liudmyla Mykolaivna Yaremenko, and О. Федорченко. "Інтерпрофесійні культурно-мистецькі обшири лікаря Кесаря Білиловського." Thesis, Сумський державний університет, 2016. http://essuir.sumdu.edu.ua/handle/123456789/49494.
Full textIn the article considered some aspects of cultural and artistic activities doctor’s Kesar Bilulovskiy at the turn of ХІХ –ХХ century, in particular, as the publisher of the almanac “Sckladka”; his medical and sanitary essays in the development of health care on the territory Russia and Ukraine and hygiene promotion, healthy lifestyles.
Mota, Aline Veras Leite. "Análise do discurso da jurisprudência do STJ nas ações de indenização por erro médico: impacto no sistema de saúde." Universidade de São Paulo, 2015. http://www.teses.usp.br/teses/disponiveis/17/17157/tde-14102015-230345/.
Full textHealthcare organizations, educational institutions, researchers and healthcare professionals have invested in mechanisms to improve the integral medical assistance offered to patients, but these assistance could have failures that may result in injury to patients, family members, and damage to system. One of the mechanisms to repair the damage is to claim to the Judiciary. In Brazil, especially since 2003, there has been an increase the lawsuit number related to medical malpractice, reflecting the changes in society and the expansion of social and fundamental rights. This is a retrospective study of judged cases by the Superior Court of Justice, in the period from 2003 to 2013, regarding the lawsuits against healthcare professionals and institutions in the public and private practice. Performed quantitative and qualitative analysis of the Superior Court of Justice Ministers speeches content, using the collective subject discourse method. Analyze of decisions contributed to understanding of the predominated issues in the malpractice lawsuit. The study identified the women as the most vulnerable to medical errors and medical specialties directly related to women\'s health as the most driven in court. Gynecology/Obstetrics (27.08%), Orthopedics (12.5%) and Plastic Surgery (10.42%) were, respectively, the most demanded specialties. In conclusion, the study provides subsidy for healthcare organizations identify potential areas of action to implement strategies to reduce the likelihood of injury to patients, decreasing costs and medical malpractice.
Silva, Natércia Fonseca de Carvalho da. "FUZZYVISA: modelo de avaliação de risco da vigilância sanitária para inspeção de resíduos de serviços de saúde utilizando lógica Fuzzy." Universidade do Estado do Rio de Janeiro, 2010. http://www.bdtd.uerj.br/tde_busca/arquivo.php?codArquivo=1711.
Full textThis study shows a health inspections model of waste management of health establishments in Rio de Janeiro state. The model was built by fuzzys logic and with experts information. It was based in ANVISA rules about waste management in health services: RSS, a RDC 306/04. It makes a simulation of an expert actuation with the diffuse elements of health inspection. The objective of this study is to show a health inspection management waste practice structured instrument, using fuzzys logic, able to optimize the inspection, produce indicators of health control to monitor the satisfactory condition of healh services waste management and guide the planning actions. The fuzzy model was developed with Matlab software and tasted with 10 inspection reports dated of 2009, between may and november.
Lécu, Anne. "L'épreuve : La « prison-pharmakon » : remède et poison." Thesis, Paris Est, 2010. http://www.theses.fr/2010PEST2014.
Full textThat which is happening to XXIst century man in prison is, in part, similar to what ishappening to all of us. Our innocence lost, (innocence is retained only by the child), we try to regain itby claiming to be the victim. We are presumed guilty, isolated, observed. Homo carceralus hauntsour Western culture; fruit of nihilism and gnosis. It is the reason we should reflect on his ordeal, notfrom the outside, but as something that could happen to each and every one of us, and in which todiscover where the poison lies and what the remedy could be. For gnosis, (either sophism ornihilism), is false when we are led to believe that we exit an ordeal by escaping our human conditionin the ‘upward’ direction of the natural sciences, statistical knowledge or technique. Resignation andheadlong pursuit share a characteristic, that of a predestined tendency towards disaster. Neither theone nor the other sits comfortably in this world or our times.But meaning does not have to come from elsewhere. If prison is pharmakon, both remedy andpoison, it is because it is a human institution. Man’s greatness is his conflicting authority : having thecapacity to overcome determinism, the ability not to resign himself to his fate, even at his lowestpoint. But it is imperative not to be left alone through this ordeal, for it is true that it is the other,particularly the ‘weakened other’, thanks to whom the crossing is possible from ‘below’. Care inprison is rooted in this ‘solidarity of the weak’. To navigate the different penitentiary and healthsystems, which seek to control and foresee the captives’ behaviour, the medical doctor must exertmêtis, become complicit with the patient in order to serve the patient. And at the same timecategorical medical confidentiality must be maintained, in the name of which the patient in his or herfragility, remains invisible to all sciences and techniques which are yet greater than he or she is. This‘secret’ knowledge is none other than Socratic knowledge: ‘I know that I do not know’
Daimaru, Ken. "Préserver la santé des armées dans le Japon moderne : la médecine militaire face à la guerre russo-japonaise." Thesis, Paris 10, 2017. http://www.theses.fr/2017PA100168.
Full textThis thesis analyses the experiences of the Russo-Japanese War (1904-1905), bringing together two historical objects of inquiry: the history of warfare and the history of medicine. Its purpose is to document and understand the organization of the Imperial Japanese Army Sanitary Corps and the medical practices that unfolded within it at the turn of the twentieth century. Focusing on the creation and the institutionalization of the care of the war wounded and sick during the Meiji era (1868-1912) and its implications for the conflict of 1904-1905, this thesis highlights the institutional and social dynamics of military medicine and the cultural production of discourses, objects and images related to war diseases and wounds. Our theoretical framework articulates the entanglement of the various actors’ perceptions (Japanese doctors and international observers) on the wounded and/or diseased body. Our results show how the transformation of the battlefield, induced by increased firepower and the resulting tactical and strategic reorganization, was also a driving force for the medicalization of combat activities, military research and the production of expertise. These processes reshaped the paradigms of combat aimed at maintaining the competitiveness of the military, that the success of preventive medicine serves to legitimize. They also accentuate the fragility of the army and the structure of medicine on the battlefield, which were under increasing stress due to the rapid progress of industrialization. The professional specialization and individual practices observed during the war lead us to discuss the benefits and limits of the strategies adopted by Japanese military surgeons to resist the increasingly destructive realities of industrial warfare
Vaněk, Ondřej. "Zdravotně technické a plynovodní instalace v obytné budově." Master's thesis, Vysoké učení technické v Brně. Fakulta stavební, 2016. http://www.nusl.cz/ntk/nusl-240328.
Full textMauck, Erin. "A Qualitative Analysis of End-of-Life Healthcare in Tennessee: Politics, Principles, and Perceptions." Digital Commons @ East Tennessee State University, 2020. https://dc.etsu.edu/etd/3846.
Full textOtt, Kenneth Brad. "The Closure of New Orleans' Charity Hospital After Hurricane Katrina: A Case of Disaster Capitalism." ScholarWorks@UNO, 2012. http://scholarworks.uno.edu/td/1472.
Full textHadačová, Jana. "Zdravotně technické a plynovodní instalace v bytovém domě se zdravotnickým zařízením." Master's thesis, Vysoké učení technické v Brně. Fakulta stavební, 2015. http://www.nusl.cz/ntk/nusl-227759.
Full textБідюкова, М. С. "Правове регулювання матеріального забезпечення працівників ОВС." Thesis, Харківський національний університет внутрішніх справ, 2008. http://essuir.sumdu.edu.ua/handle/123456789/51722.
Full textEssence of legal relation of policemen’s salary maintenance is elucidated in this research work; its notion is determined. Principles of policemen’s salary maintenance are viewed. Modern state of legal regulation of policemen’s salary maintenance is analyzed. Essence and peculiarities of separate kinds of policemen’s salary maintenance such as payment, privileges and compensations, state obligatory personal insurance, housing guaranteeing, medical and health resort guaranteeing, pension guaranteeing are elucidated. Concrete propositions and recommendations as for improving policemen’s salary maintenance are presented.
Lucas, D. Pulane. "Disruptive Transformations in Health Care: Technological Innovation and the Acute Care General Hospital." VCU Scholars Compass, 2013. http://scholarscompass.vcu.edu/etd/2996.
Full textYeh, Ching-Chung, and 葉慶仲. "AN OPTIMIZATION MODEL FOR MANPOWER ASSIGNMENT TO OFFICIAL AUDITING IN SANITARY AFFAIRS." Thesis, 2008. http://ndltd.ncl.edu.tw/handle/4f36hp.
Full text國立中央大學
土木工程學系碩士在職專班
96
The economy of our country grows vigorously in recent year. It makes the national income raised and the life style of society’s living changed. The concession related to sanitation is increasing constantly. The sanitary issue that people forgather in concession has an increasing drift. In order to insure the health of nationals, the officials have to enhance the auditing activities of various kinds of hygienic condition of concession. The arrangement of auditing manpower which was not an optimistic arrangement was usually made artificially in the pastime. The front office usually takes much time to deal with in the past as well. The most important issue that front office concerns is to keep the manpower arrangement optimistic and fair. We develop an optimistic manpower assignment’s model with the aid of computer programming to resolve the minimum working days of auditor and the combination of manpower assignment according to the study focusing on the sanitary auditing activities for the Sanitation Office. The susceptibility of the parameters act on the minimum working days help us to realize that the minimum working days change by the parameters have been setted in this model. After case studying, we find that the manpower assignment model is superior to artificial method. The results reveal that the optimistic model looks after benefit and fairness of manpower assignment. It can be the manpower assignment’s reference of officials in practice.
Hou, Ming-chien, and 侯名謙. "The Study of Applying Radio Frequency Identification to Medical Affairs." Thesis, 2005. http://ndltd.ncl.edu.tw/handle/93368594125302175270.
Full text義守大學
資訊管理學系碩士班
93
Radio Frequency Identification (RFID) has become very suitable for medical affairs because of its low-power transmitting frequency and wireless tracking characteristic. It has currently been used in many medicine centers for tracking highly contagious patients. For addressing the issues of accurately tracking patients’ locations, reducing the communication cost of existing RFID systems, and occupying less database space, this research refers to the architecture of the current mobile communication system and proposes a hierarchical RFID architecture, different from the current one. The proposed architecture can locate patients’ current positions more accurately and reduce locating delay greatly. Based on patients’ moving regularity under a medical environment, this research will also modify the original concurrent search algorithm in mobile communication to efficiently find RFID tags on the proposed hierarchical RFID architecture. At last, a program for collecting patients’ actual moving positions and frequencies will be designed to validate the performance of the modified concurrent search algorithm in locating patients’ positions. In summary, this research hopes to help understand the contribution of RFID to the medicine field by planning and implementing an RFID system.