RESUMEN
El control interno de calidad en el laboratorio clínico es una actividad especializada que monitoriza la calidad de los procesos y resultados, a la vez que permite aceptar o rechazar las corridas analíticas de las diferentes determinaciones. A tales efectos, se presentan los elementos de una guía práctica incluida en un software, diseñada con el objetivo de perfeccionar el control interno de la calidad en dichos laboratorios, donde se definen los principios y conceptos claves del tema, los procedimientos y su secuencia, los requisitos de calidad, las reglas de control, los cálculos estadísticos, la interpretación de los resultados, así como algunos de los indicadores novedosos y necesarios para asegurar la calidad.
The internal control of quality in the clinical laboratory is a specialized activity that monitors the quality of the processes and results at the same time that it allows to accept or to reject the analytic runs on the different determinations. To such effects, the elements of a practical guide included in a software are presented, designed with the objective of perfecting the internal control of the quality in these laboratories, where the principles and key concepts of the topic, procedures and their sequence, requirements of quality, control rules, statistical calculations, the interpretation of the results are defined, as well as some of the novel and necessary indicators to assure the quality.
Asunto(s)
Gestión de la Calidad Total , Laboratorios Clínicos , Control de CalidadRESUMEN
Chinese medicine (CM) is the most typical conventional therapy compared with any other traditional or alternative medicine systems. The active components of CMs are either primary or secondary metabolites generated by metabolic and biosynthetic enzymes in plants, protecting the plants from environmental stress. The characteristics of these metabolites are diverse, complicated and unique. In this paper, current approaches for quality assessment were extensively reviewed, a new concept of quality marker (Q-marker) was then proposed for CM quality assessment. Additionally, definition of the Q-marker, as well as the relevant methods, were discussed, on the basis of the biosynthetic pathways of secondary metabolites and source of biological active components. Study design of Q-marker is complex system for quality assessment and production process control of CM products with transitivity and traceability. Therefore, the system with characteristics of transmission and traceability is expected to be established for regulation of quality. Upon the concept which the transitivity and traceability in the quality assessment and production process control covered the entire process, such as raw materials, decoction slices, processing, extraction and production can be further enhanced. The transitivity and traceability will inevitably require close attention to “who, what, where, when, and why” details at each stage of Q-markers of CM production form raw materials to patent product. The establishing quality standards are enablers of many and various transitivity and traceability solutions, not a solution in them. It means that the transitivity and traceability system is readily link between products and across borders in quality. According to the thinking mode and methods of investigation on quality assessment of CM product, we focus on the entire process, in terms of safety and effectiveness and quality control. The standard preparation of CM or CM decoction is not only the basis for study of Q-marker, but also the basis for transmission and traceability of the quality of CM product.
RESUMEN
To promote the healthy development of pharmaceutical industry, improve the quality standard system, core of national pharmacopoeia standards, and product quality standards of Chinese materia medica (CMM), we analyzed the existing quality assessment methods and problems on the proposed new concept on Chinese medicine quality markers. On this basis, the factors affecting the quality of CMM and secondary metabolites, herbal product quality and quality standards and regulatory problems in the quality of the material basis of CMM to determine the definition of quality markers of CMM, and research methods in terms of quality evaluation of applications to discuss with colleagues. For a common goal, we would like to respond to this concept can lead counterparts.
RESUMEN
OBJECTIVE To diminish and discontinue intra-hospital cross infection in Disinfection Supplier Centre.METHODS The administration of personal resources control was developed,the equipment and systemic control of aseptic process and isolation was reasonably arranged,and the quality control was enhanced.We executed the routine seriously during our daily work,and gave strict measures during quality management such as disposal,classification,washing,disinfection,packaging,sterilization,monitoring,stockpile,and handout.RESULTS Every criterion of aseptic and isolation work were all adapted to the demanding set up by Ministry of Health referred to hospital infection control quality standard,The infection control in our Centre was standardized and regular scientific channel was set up.CONCLUSIONS Quality administration care can play a main and key role in the control of cross hospital infection in Disinfection Supplier Centre.
RESUMEN
The effect and value that are assurance of standard operation in quality control and administration of digital im- ages were discussed. The putting forward concept and aim of standard operation were classified into four grades: best, good, checkout and below standard according to evaluating factors and conditions of standard operation. In order to guarantee the implementation of quality control, medical staff should renew ideas and enhance the consciousness of quality control. The standard operation can be guided and supervised by the director in machine and the system of rewards and penalties can be established. The standard operation has important significance and values, which carry out quality control and quality ad- ministration in medical imaging effectively.