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Consultoría de Implantación de Sistemas Informáticos


 
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¿Cuál es el sistema mas adecuado para mi organización?
Esta es la pregunta clave a la hora de implementar un sistema informático en entorno GMP; no siempre el sistema tecnológicamente mejor se corresponde a la elección acertada.
El éxito se persigue a partir de la correcta definición del proyecto de implementación.
en SEV hemos participado en un gran número de proyectos de implementación de sistemas informáticos, y sabremos guiarte en la definición de tus requisitos de usuario, en la selección del proveedor y en la sucesiva gestión del cambio asociado con la introducción del nuevo sistema.

Referencias

Equipment used in the manufacture, processing, packing, or holding of a drug product shall be of appropriate design, adequate size, and suitably located to facilitate operations for its intended use and for its cleaning and maintenance.

21 CFR Part 211, Sec 211.63

Validation should be considered as part of the complete life cycle of a computer system. This cycle includes the stages of planning, specification, programming, testing, commissioning, documentation, operation, monitoring and modifying.

EU GMP, Annex 11, Computerized Systems

The manufacturer shall establish and implement an effective pharmaceutical quality assurance system, involving the active participation of the management and personnel of the different departments.

COMMISSION DIRECTIVE 2003/94/EC, Article 6

It is a requirement of GMP that manufacturers identify what validation work is needed to prove control of the critical aspects of their particular operations. Significant changes to the facilities, the equipment and the processes, which may affect the quality of the product, should be validated. A risk assessment approach should be used to determine the scope and extent of validation.

EU GMP, Annex 15, Qualification and validation