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Presencial / Streaming

This course aims to combine the requirements of ISO 17025 for laboratories with the application requirements of ISO 27001, given the growing importance of confidentiality, maintenance, and integrity of records, as well as the risks associated with their loss. It is a compilation of best practices for implementing security management measures, specifically focused on laboratories, which protect information and assure clients that their data is secure.

e-Learning, Presencial / Streaming

We will introduce you to the minimum parameters to consider for the proper definition of a chromatographic method and for establishing its controls. The concept of Instrumental Calibration will be reviewed in its different approaches (curve fitting with multiple points, use of the response factor, with and without internal standard, with and without matrix) along with the criteria for its evaluation. We will explain the validation parameters (linearity, trueness, and precision) and the estimation of the uncertainty of the results.

e-Learning, Presencial / Streaming

We will introduce you to the minimum parameters to consider for the proper definition of an ICP-MS method and its control. The concept of Instrumental Calibration will be reviewed in its different approaches (curve fitting with multiple points, use of the response factor, with and without internal standard, with and without matrix) and the criteria for its evaluation. We will clarify and work on the validation parameters (linearity, trueness, and precision) as well as the estimation of the uncertainty of the results.

Presencial / Streaming

Not only are concepts and requirements related to the need for laboratories to carry out scheduled internal audits reviewed, but a practical component is also included, divided into the different phases of conducting an audit. The course focuses on the need for training and qualification of potential internal auditors. To ensure the effectiveness of audits, some clarifications from the UNE–EN ISO 19011:2018 “Guidelines for Auditing Management Systems” standard are also provided.

e-Learning

It is important to clarify good practices within a laboratory, regardless of the type of laboratory or the tests performed. It is also essential to understand the categories of non-hazardous waste that may be generated, as well as the different categories of hazardous waste and their incompatibilities. Knowing how to respond to accidents or incidents related to waste management is crucial. In addition, it is necessary to explain the proper procedures for transferring and handling generated waste. Understanding waste classifications according to applicable regulations, as well as their identification and labeling, is fundamental. All of these aspects aim to provide an appropriate management system for laboratories based on their waste generation, ensure the proper functioning of a laboratory—even in the management of hazardous or non-hazardous waste—and guarantee that waste management is carried out correctly and in compliance with current legislation.

e-Learning, Presencial / Streaming

Os indicamos en qué ha variado la nueva ISO 11731:2017 y cómo adaptar los nuevos cambios siguiendo un Sistema de Calidad. Abordamos las pautas a seguir si ya tienes el método validado y/o acreditado. Con ejemplos prácticos que surgen de la aplicación de los nuevos planteamientos de la norma y que dependen del tipo de matriz, carga bacteriana acompañante / Legionella spp. esperada y límite de detección teórico asociado a los tipos de siembra y tratamientos.

e-Learning, Presencial / Streaming

We explain the changes introduced in the new ISO 11731:2017 and how to adapt to them within a Quality System. We cover the guidelines to follow if you already have the method validated and/or accredited. Practical examples are provided based on the application of the new requirements of the standard, depending on the type of matrix, expected accompanying bacterial load/Legionella spp., and the theoretical detection limit associated with the types of inoculation and treatments.

Presencial / Streaming

La detección y cuantificación de Legionella spp. en aguas es un requisito fundamental en la prevención de la legionelosis y está regulada por el Real Decreto 487/2022, que establece las condiciones sanitarias para su control. La norma ISO 11731:2017 define el método de referencia para el recuento de Legionella spp. mediante cultivo, siendo el estándar utilizado para el análisis microbiológico en laboratorios acreditados.

Para lograr la acreditación ISO 17025, los laboratorios deben cumplir con exigencias específicas relacionadas con la competencia técnica, control del entorno, calibración y verificación de equipos, medios de cultivo y gestión de la calidad del ensayo.

En este curso, abordaremos los requisitos clave para la acreditación, desde la preparación del laboratorio hasta la interpretación de resultados y emisión de informes, incluyendo los procedimientos de verificación del métodocontroles de calidad internos y externos y la correcta gestión documental.

Presencial / Streaming

El objetivo principal del curso es ofrecer una visión clara, práctica y útil sobre cómo aplicar los principios ESG en las organizaciones, incluidos Laboratorios de ensayo, tomando como base la guía IWA 48. A lo largo del curso, los participantes aprenderán a identificar riesgos relevantes, trabajar con las partes interesadas, integrar la sostenibilidad en los procesos de la organización y definir indicadores que permitan medir avances reales.

e-Learning, Presencial / Streaming

In any organization, non-compliance with applicable requirements may arise in the course of daily activities (reference standards, customer requirements, regulatory obligations, etc.), which in some cases may even call into question the quality of the work itself or its technical competence. ENAC Operational Note 11 (NO-11) is the document that, among other aspects, describes the method established by ENAC, the Spanish National Accreditation Body, for classifying nonconformities according to their severity, as detected during the accreditation processes of a conformity assessment body (CAB), such as Testing and Calibration Laboratories, Inspection Bodies, etc. In this training, we help you to clearly understand the key concepts, as well as the steps to follow for the correct management of nonconformities and corrective actions, so that you can optimize the process and consider it the best tool for problem-solving.