Manual de Gestión de la Calidad ISO 17025:2017 MGC-001

The document is divided into several sections, each addressing a specific aspect of laboratory management. The laboratory's objective is to provide accurate and reliable results, and to maintain a high level of quality in its services. To achieve this, the laboratory must have a clear understanding of its scope and the requirements of its clients. The laboratory must have a management system in place that is based on the principles of ISO 17025:2017. This system must include procedures for the management of quality, including the identification and control of risks, the management of non-conforming products, and the handling of complaints. The laboratory must also have a clear understanding of its responsibilities and the responsibilities of its personnel. This includes the identification of the personnel responsible for each task, the communication of responsibilities, and the training of personnel. The laboratory must have a system in place for the management of its resources, including personnel, equipment, and facilities. This system must include procedures for the selection, training, and evaluation of personnel, the maintenance and calibration of equipment, and the control of facilities. The laboratory must also have a system in place for the management of its products and services, including the identification of products and services, the management of non-conforming products, and the handling of complaints. The laboratory must have a system in place for the management of its processes, including the identification of processes, the management of non-conforming products, and the handling of complaints. This system must include procedures for the review of requests, offers, and contracts, and the evaluation of conformity. The laboratory must have a system in place for the management of its external products and services, including the identification of products and services, the management of non-conforming products, and the handling of complaints. This system must include procedures for the acquisition of products and services, the communication of requirements to suppliers, and the evaluation of conformity. The laboratory must have a system in place for the management of its products and services, including the identification of products and services, the management of non-conforming products, and the handling of complaints. This system must include procedures for the review of requests, offers, and contracts, and the evaluation of conformity. The laboratory must have a