Farmacia Aguilar

Este Blog esta destinado a compartir conocimiento relacionado con:

Tecnología Farmacéutica,
Farmacia Industrial y Galénica,

La industria Farmacéutica

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BLOGS FARMACEUTICOS

domingo, 6 de junio de 2010

KAIZEN

Origins and Definition of Kaizen
In the U.S. kaizen is often synonymous with "Kaizen Blitz" or "Kaizen Event." Such events rapidly implement workcells, improve setups or streamline processes. However, a better Japanese word for this activity is kaikaku
In Japanese, the definition of Kaizen is "improvement" and particularly, "Continuous Improvement"-- slow, incremental but constant. Norman Bodek explains this and translates it as "Quick & Easy Kaizen".
Taiichi Ohno and Shigeo Shingo developed both kaizen versions at Toyota. They are important tools for Lean Manufacturing, the Toyota Production System (TPS), Just In Time (JIT) and other effective manufacturing strategies.
Large-Scale Vs. Small-Scale Improvement
Large scale improvement is attractive. It promises quantum jumps in productivity, quality and effectiveness. However, it is difficult to implement because it affects many areas, people and processes. The design must be near-perfect because failure courts disaster. The risks and difficulties work against large-scale improvements.
Small-scale improvements are easier and faster. The risks are low because they generally have limited effect. However, the accumulated effect is often greater than a single large improvement. The Kaizen Blitz is a localized, smaller scale improvement and Mini-Kaizen are very small-scale improvements.

The Kaizen Blitz
The Blitz or Event is a focused, intense, short-term project to improve a process. Substantial resources- Engineering, Maintenance, Cell Operators, and others are available for immediate deployment.
An event usually includes training followed by analysis, design, and re-arrangement of a product line or area. A consultant often orchestrates. The Event normally takes 2-10 days. The results are immediate, dramatic and satisfying.
Mini Kaizen
Before the recent popularity of the Blitz, kaizen meant "Continuous Improvement." This is the slow accumulation of many small developments in processes and quality that, over 50 years, has helped make Toyota the lowest cost and highest quality automobile company in the world. Let's call these improvements "Mini Kaizen."
Mini Kaizen is part of corporate culture. It requires both conscious and sub-conscious thinking about improvements day by day and minute by minute on the part of all employees. It also requires that these same employees possess the skills for this type of thinking.
The mini variation is far more difficult to keep up and takes much longer for results than a blitz. But, as Toyota has demonstrated, it offers a more sustained competitive advantage.

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Bienvenida

El concepto de Tecnología Farmacéutica Industrial, se encuentra intimamente ligado al de Farmacia Galénica en cuanto a serie de procesos tecnológicos a seguir para la obtención de un medicamento estable, seguro y eficaz, es decir, de calidad. La farmacia preparativa, núcleo central de la Farmacia Galénica, ha derivado de ser magistral a ser industrial debido al cambio que la técnica moderna ha impreso en los actuales métodos de trabajo. Esta derivación de lo manual a lo mecánico, de lo magistral a lo industrial, se ha visto reflejada también en la terminología farmacéutica utilizada. Así, la palabra tecnología (“Tecnos”= Arte, “Logia”= Tratado) seguida del vocablo “farmacéutica”, expresa la parte de la Farmacia Galénica dedicada al arte de elaborar medicamentos; si a ello se suma la palabra “industrial”, se tiene que dicho arte farmacéutico se aplica al medicamento industrializado, es decir, al medicamento que será elaborado de forma seriada y contínua en instalaciones de gran volumen. Este hecho ha provocado un lógico cambio en el planteamiento de la investigación galénica tendente a la obtención de un nuevo medicamento, entendiendo como tal al principio activo medicamentoso dotado de una forma farmacéutica y dispuesto para su administración al paciente. En efecto, es necesario plantear inicialmente una caracterización del principio activo medicamentoso que debe ser convertido en medicamento, desarrollar unos preceptivos estudios de preformulación, diseñar unas formulaciones base a partir de las cuales pueda definirse una formulación definitiva, establecer la tecnología de fabricación óptima y los controles en proceso a efectuar para asegurar la calidad del producto final, validar dicha tecnología, establecer unos controles de producto acabado con sus correspondientes especificaciones y, finalmente, desarrollar los perceptivos estudios de estabilidad del medicamento que den a conocer el período de caducidad del mismo. Por tanto este tipo de investigación e información es el que se brinda en esta web por parte del autor Johnny Aguilar.