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Validación de Sistemas Informatizados


 
Muevete hacía la dirección correcta



Al igual que en la industria farmacéutica, en la industria cosmética también existen multitud de sistemas que se emplean en la gestión de las operaciones empresariales más críticas:
- Gestión de almacenes (existencias, estados de lotes...).
- Gestión de la producción (gestión de recetas, dispensing...).
- Gestión documental (PNTs, registros de formación...).
- Control de calidad (controles de materias primas, de producto terminado...)
- [...]
SEV pone a su disposición toda su experiencia en validación de sistemas informáticos adquirida a lo largo de los múltiples proyectos realizados en la industria farmacéutica.

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