Buscar
Mostrando ítems 1-10 de 1424
Potentiometric determination of captopril in pharmaceutical formulations
(Editora Unesp, 2003-01-01)
A simple, precise, rapid and low-cost potentiometric method for captopril determination in pure form and in pharmaceutical preparations is proposed. Captopril present in tablets containing known quantity of drug was ...
Infrared imaging spectroscopy and chemometric tools for in situ analysis of an imiquimod pharmaceutical preparation presented as cream
(Pergamon-elsevier Science LtdOxfordInglaterra, 2014)
Comments On “the Organization Of Pharmaceutical Services By ‘health Region’ In Brazil’s Unified Health System”
(Associacao Brasileira de Pos - Graduacao em Saude Coletiva, 2017)
Pharmaceutical impurities and degradation products: Uses and applications of NMR techniques
(Elsevier, 2014-04)
Current standards and regulations demand the pharmaceutical industry not only to produce highly pure drug substances, but to achieve a thorough understanding of the impurities accompanying their manufactured drug substances ...
From The System’s Organization To The Fragmentation Of Care: Perception Of Users, Doctors And Pharmacists About The Specialized Component Of Pharmaceutical CareDa Organização Do Sistema à Fragmentação Do Cuidado: A Percepção De Usuários, Médicos E Farmacêuticos Sobre O Componente Especializado Da Assistência Farmacêutica
(Institute de Medicina Social da UERJ, 2016)
Armazenamento de medicamentos na Central de Abastecimento Farmacêutico (CAF) de um município do Rio Grande do Norte, Brasil
(Conselho Federal de Farmácia - CFF, 2019-12-31)
Medicines represent solve most of the health problems. Preservation of its quality should be guaranteed from manufacturing to dispensing to the patient. In this sense, the present study aims to analyze the process of drug ...
Analytical Validation of Quantitative High-Performance Liquid Chromatographic Methods in Pharmaceutical Analysis: A Practical Approach
(Taylor & Francis Inc, 2012-01-01)
Analytical validation is an essential component in allowing a laboratory to ensure routine acceptable performance of analytical methods. Despite the considerable amount of important published work on this subject, diversity ...