RESUMO
The analytical procedure life cycle (APLC) provides a holistic framework to ensure analytical procedure fitness for purpose. USP's general chapter <1220> considers the validation activities that take place across the entire analytical procedure lifecycle and provides a three-stage framework for its implementation. Performing ongoing analytical procedure performance verification (OPPV) (stage 3) ensures that the procedure remains in a state of control across its lifecycle of use post validation (qualification) and involves an ongoing program to collect and analyze data that relate to the performance of the procedure. Knowledge generated during stages 1 (procedure design) and 2 (procedure performance qualification) is used as the basis for the design of the routine monitoring plan to support performance verification (stage 3). The extent of the routine monitoring required should be defined based on risk assessment, considering the complexity of the procedure, its intended purpose, and knowledge about process/procedure variability. The analytical target profile (ATP) can be used to provide or guide the establishment of acceptance criteria used to verify the procedure performance during routine use (e.g., through a system/sample suitability test (SST) or verification criteria applicable to procedure changes or transfers). An ATP however is not essentially required to perform OPPV, and a procedure performance monitoring program can be implemented even if the full APLC framework has not been applied. In these situations, verification criteria can be derived from existing validation or system suitability criteria. Elements of the life cycle approach can also be applied retrospectively if deemed useful.
RESUMO
El agua, dentro de la industria farmaceutica, es el excipiente de mayor uso. En los ultimos años, con el advenimiento de nuevas tecnologias, los metodos analiticos utilizados para evaluar la calidad del agua han evolucionado simplificandose en su numero, aunque requiriendo nuevos equipamientos. Se brindan los requisitos oficiales para el agua de uso farmaceutico y consideraciones sobre el control microbiológico
Assuntos
Argentina , Qualidade da Água , Indústria FarmacêuticaRESUMO
El agua, dentro de la industria farmaceutica, es el excipiente de mayor uso. En los ultimos años, con el advenimiento de nuevas tecnologias, los metodos analiticos utilizados para evaluar la calidad del agua han evolucionado simplificandose en su numero, aunque requiriendo nuevos equipamientos. Se brindan los requisitos oficiales para el agua de uso farmaceutico y consideraciones sobre el control microbiológico
