{"id":3221,"date":"2024-02-28T12:05:00","date_gmt":"2024-02-28T18:05:00","guid":{"rendered":"https:\/\/www.adecom.com.mx\/?post_type=tribe_events&p=3221"},"modified":"2024-03-28T09:34:15","modified_gmt":"2024-03-28T15:34:15","slug":"interpretacion-de-la-norma-iso-iec-170252017","status":"publish","type":"tribe_events","link":"https:\/\/www.adecom.com.mx\/en\/event\/interpretacion-de-la-norma-iso-iec-170252017\/","title":{"rendered":"Interpretaci\u00f3n de la Norma ISO\/IEC 17025:2017"},"content":{"rendered":"

Incrementa tus conocimientos y los de tu equipo de trabajo con este curso sobre Norma ISO\/IEC 17025. En ADECOM desarrollamos programas especializados en Torque y Metrolog\u00eda para fortalecer la educaci\u00f3n en nuestro pa\u00eds. Con la disponibilidad de impartir cursos de forma presencial en tus instalaciones o de forma virtual. Conoce el temario de este curso:<\/strong><\/p>\n

 <\/p>\n

Objetivo:<\/strong><\/p>\n

Al terminar el curso los asistentes ampliaran sus conocimientos metrol\u00f3gicos y normativos aplicables de manera pr\u00e1ctica , l\u00f3gica y consistente en el sector en el que desarrollen sus actividades , as\u00ed como conocer y entender \u00a0los est\u00e1ndares y principios de medici\u00f3n, trazabilidad metrol\u00f3gica y requerimientos normativos en ISO EC 17025.<\/p>\n

 <\/p>\n

TEMARIO<\/p>\n

    \n
  1. Gesti\u00f3n de la calidad en un laboratorio: Conceptos generales<\/strong><\/li>\n<\/ol>\n
      \n
    • Sistemas de gesti\u00f3n de calidad en un laboratorio<\/li>\n
    • Generalidades de la norma ISO\/IEC 17025:2017<\/li>\n
    • Norma ISO 17025 versus iso 9000<\/li>\n
    • Documentaci\u00f3n del sistema<\/li>\n
    • Aspectos generales de la acreditaci\u00f3n<\/li>\n
    • Documentos de referencia<\/li>\n<\/ul>\n
        \n
      1. Requisitos relativos a la estructura<\/strong><\/li>\n<\/ol>\n
          \n
        • Introducci\u00f3n<\/li>\n
        • T\u00e9rminos y definiciones<\/li>\n
        • Requisitos generales<\/li>\n
        • Requisitos relativos a la estructura<\/li>\n<\/ul>\n
            \n
          1. Requisitos relativos a los recursos<\/strong><\/li>\n<\/ol>\n
              \n
            • Introducci\u00f3n<\/li>\n
            • Personal<\/li>\n
            • Instalaciones y condiciones ambientales<\/li>\n
            • Equipamiento<\/li>\n
            • Trazabilidad metrol\u00f3gica<\/li>\n
            • Productos y servicios suministrados externamente<\/li>\n<\/ul>\n
                \n
              1. Requisitos del proceso: Parte 1<\/strong><\/li>\n<\/ol>\n
                  \n
                • Introducci\u00f3n<\/li>\n
                • Revisi\u00f3n de solicitudes, ofertas y contratos<\/li>\n
                • Selecci\u00f3n, verificaci\u00f3n y validaci\u00f3n de m\u00e9todos<\/li>\n
                • Muestreo<\/li>\n
                • Manipulaci\u00f3n de los \u00edtems de ensayo o calibraci\u00f3n<\/li>\n
                • Registros t\u00e9cnicos<\/li>\n
                • Evaluaci\u00f3n de la incertidumbre de medici\u00f3n<\/li>\n<\/ul>\n
                    \n
                  1. Requisitos del proceso. Parte 2<\/strong><\/li>\n<\/ol>\n
                      \n
                    • Introducci\u00f3n<\/li>\n
                    • Aseguramiento de la validez de los resultados<\/li>\n
                    • Informe de resultados<\/li>\n
                    • Quejas<\/li>\n
                    • Trabajo no conforme<\/li>\n
                    • Control de los datos y gesti\u00f3n de la informaci\u00f3n<\/li>\n<\/ul>\n
                        \n
                      1. Requisitos relativos al sistema de gesti\u00f3n<\/strong><\/li>\n<\/ol>\n
                          \n
                        • Introducci\u00f3n<\/li>\n
                        • Opciones<\/li>\n
                        • Documentaci\u00f3n del sistema de gesti\u00f3n<\/li>\n
                        • Control de los documentos del sistema de gesti\u00f3n<\/li>\n
                        • Control de los registros<\/li>\n
                        • Acciones para abordar riesgos y oportunidades<\/li>\n
                        • Mejora<\/li>\n
                        • Acciones correctivas<\/li>\n
                        • Auditor\u00edas internas<\/li>\n
                        • Revisiones por la direcci\u00f3n<\/li>\n<\/ul>\n
                            \n
                          1. Requisitos de acreditaci\u00f3n<\/strong><\/li>\n<\/ol>\n
                              \n
                            • La acreditaci\u00f3n<\/li>\n
                            • Los Organismos Acreditadores<\/li>\n
                            • Proceso de Acreditaci\u00f3n<\/li>\n
                            • Proceso de acreditaci\u00f3n en Espa\u00f1a y Europa<\/li>\n
                            • Proceso de acreditaci\u00f3n en Am\u00e9rica<\/li>\n<\/ul>\n

                              8. Documentaci\u00f3n del sistema<\/strong><\/p>\n

                               <\/p>\n

                              Sesi\u00f3n de preguntas y respuestas<\/strong><\/p>\n

                               <\/p>\n

                              Evaluaci\u00f3n: <\/strong>Al final del curso se aplicar\u00e1 una breve evaluaci\u00f3n de 10 puntos, para determinar el nivel de entendimiento de cada asistente.<\/p>\n

                               <\/p>\n

                              Reconocimiento: <\/strong>Al final del curso, a cada asistente que haya concluido de forma satisfactoria se le entregar\u00e1 una constancia de participaci\u00f3n.<\/p>\n

                               <\/p>\n

                              Generalidades<\/strong><\/p>\n

                              Duraci\u00f3n: 4 horas<\/p>\n

                              Horario: 8:00am – 12:00pm<\/p>\n

                              Pre-requisitos: Calidad visual y auditiva aceptable de cada participante. Servicio de internet estable. Responder evaluaci\u00f3n diagn\u00f3stica 48 horas previas al curso.<\/p>\n

                               <\/p>\n

                              Parte de las credenciales de nuestro ponente:<\/strong><\/p>\n

                                \n
                              • Certificaci\u00f3n de auditor l\u00edder ISO 9001:2015<\/li>\n
                              • 8 DISCIPLINAS \u2013 METODOLOG\u00cdA PARA LA SOLUCI\u00d3N DE PROBLEMAS<\/li>\n
                              • Certificado en Core Tools (MSA, SPC, APQP \u2013 PPAP,\u00a0AMEF) para el sector automotriz.<\/li>\n
                              • Auditor L\u00edder es ISO 9001:2015<\/li>\n
                              • Auditor de segunda Parte en Sistema de Gesti\u00f3n de la Calidad, ISO 9001:2015 + IATF 16949:2016<\/li>\n<\/ul>\n

                                 <\/p>\n

                                **Este evento es virtual y se emite en vivo, no es grabado**<\/p>\n

                                 <\/p>\n

                                \"\"<\/p>","protected":false},"excerpt":{"rendered":"

                                Incrementa tus conocimientos y los de tu equipo de trabajo con este curso sobre Norma ISO\/IEC 17025. En ADECOM desarrollamos programas especializados en Torque y Metrolog\u00eda para fortalecer la educaci\u00f3n […]<\/p>\n","protected":false},"author":4,"featured_media":3226,"template":"","meta":{"_acf_changed":false,"content-type":"","_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"episode_type":"","audio_file":"","podmotor_file_id":"","podmotor_episode_id":"","cover_image":"","cover_image_id":"","duration":"","filesize":"","filesize_raw":"","date_recorded":"","explicit":"","block":"","_tribe_events_status":"","_tribe_events_status_reason":"","_joinchat":[],"footnotes":""},"tags":[],"tribe_events_cat":[],"class_list":["post-3221","tribe_events","type-tribe_events","status-publish","has-post-thumbnail","hentry"],"acf":[],"yoast_head":"\nInterpretaci\u00f3n de la Norma ISO\/IEC 17025:2017 - Adecom<\/title>\n<meta name=\"description\" content=\"Curso en l\u00ednea Norma ISO 17025 2017. 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