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Projeto para automação de tanque de formulação de vacinas
(Universidade Tecnológica Federal do ParanáCuritibaDepartamento Acadêmico de Eletrônica, 2014-12-03)
This paper presents an automation project of a vaccine formulation tank that meets the quality requirements for utilization in a pharmaceutical company. The automation application in this tank will ensure the correct ...
Controle de qualidade microbiológico de produtos farmacêuticos não estéreis
(Universidade Federal de Minas GeraisUFMG, 2012-10-23)
Quality control is part of Good Manufacturing Practices (GMP), that arerelevant and necessary for that pharmaceuticals are not released for sale or supply until their quality is considered satisfactory. The present study ...
Diseño del área de farmacotecnia para fórmulas magistrales no estériles en el servicio de farmacia del Hospital Andino de la ciudad de Riobamba.
(Escuela Superior Politécnica de Chimborazo, 2018-05)
The objective of this degree was the design of the area of pharmaceutical magisterial non-sterile formulations in the Hospital Andino, Pharmacy of Riobamba. This design is the result of an assessment to the current conditions ...
Topical vaccination with super-stable ready to use nanovesicles
(Elsevier Science, 2017-04)
Ultradeformable archaeosomes (UDA) are nanovesicles made of total polar archaeolipids (TPA) from the archaea Halorubrum tebenquichense, soybean phosphatidylcholine and sodium cholate (3:3:1 w/w). Fresh dispersions of UDA ...
Intravenous Administration: Technological Considerations
(Springer, 2021)
Dosage forms are pharmaceutical finished products, containing one or more active ingredients (drug), in a specified dose, and several inactive ingredients or excipients. When given to the patient by an adequate route of ...
Choice of sterilizing/disinfecting agent - determination of the Decimal Reduction Time (D-Value)
(Univ Sao Paulo, Conjunto QuimicasSao PauloBrasil, 2009)