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Servicios

Sistemas de Control


 
Todas las piezas en su sitio



Los sistemas de producción han evolucionado, a lo largo de las últimas decadas, de forma impresionante; ya es impensable implementar maquinarias o lineas de producción que no tengan sus sistemas de control automáticos.
Todos estos sistemas gestionan parámetros de funcionamiento que afectan, en muchos casos, a la calidad de los productos finales.
En esta categoría se pueden incluir los sistemas de control de accesos y climatización.
La validación de estos sistemas es obligatoria, según las normativas GMP.

SEV dispone de profesionales con amplia experiencia de validación de todo tipo de sistemas de control.

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