O papel do Quality by design na cadeia de suprimentos desverticalizada e globalizada da indústria farmacêutica

Detalhes bibliográficos
Ano de defesa: 2017
Autor(a) principal: Dias, Claudia Maria Alves de Souza de Oliveira
Orientador(a): Não Informado pela instituição
Banca de defesa: Não Informado pela instituição
Tipo de documento: Tese
Tipo de acesso: Acesso aberto
Idioma: por
Instituição de defesa: Universidade Federal do Rio de Janeiro
Brasil
Instituto Alberto Luiz Coimbra de Pós-Graduação e Pesquisa de Engenharia
Programa de Pós-Graduação em Engenharia de Produção
UFRJ
Programa de Pós-Graduação: Não Informado pela instituição
Departamento: Não Informado pela instituição
País: Não Informado pela instituição
Palavras-chave em Português:
Link de acesso: http://hdl.handle.net/11422/10146
Resumo: Pharmaceutical industries operate under several organized relational arrangements, in a geographically dispersed manner, tightly regulated and globally coordinated. Production processes can be shared by company headquarters and its subsidiaries, or even with two or more different organizations contracted in the same country or in different continents. Multiple derivative partnerships (technology transfer, technology partnerships, contracting of services, joint development, etc.), established inshore or offshore, incur greater quality risks. Based on the conceptual framework research of Quality by Design, the central issue: “if and how this artifact provides real coordination gains in the context of the current outsourced configuration of pharmaceutical supply chain, thus promoting superior articulation among the agents” was postulated. Integration of the central theme, with other theoretical approaches, was also explored and supported by literature review, a research protocol was developed and addressed to experts in the pharmaceutical industry, who ratified the complexity of the contemporary outsourced landscape and understand in that the Quality by Design approach is of great relevance in the improvement of processes and products, sharing knowledge and reducing quality risks, with the potential to minimize transactions asymmetry, as well as reducing costs of coordinating pharmaceutical supply chain.