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Instrumental Technique: Chromatography

e-Learning, In-Person / 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.

Instrumental Technique: ICP-MS

Scheduled Courses

e-Learning, In-Person / 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.

Internal Audits (Theoretical-Practical)

Scheduled Courses

In-Person / 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.

Internal Physico-Chemical Quality Control

Spreadsheets and Procedures

Laboratory Waste Management

Scheduled Courses

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.

Legionella spp Count (ISO 11731:2017) and Identification of Legionella pneumophila

Spreadsheets and Procedures

Legionella spp. According to UNE–EN ISO 11731:2017

Scheduled Courses

e-Learning, In-Person / 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.

Legionella spp. by culture (ISO 11731:2017): Key Steps to Achieve ISO 17025 Accreditation

Scheduled Courses

In-Person / Streaming

Legionella Validation by PCR (ISO 12869:2019)

Spreadsheets and Procedures

Management of non-conformities and corrective actions (ENAC NO-11)

Scheduled Courses

e-Learning, In-Person / 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.

Measurement Uncertainty in Dispenser Verification

Spreadsheets and Procedures

Measurement Uncertainty in Pressure Gauge Verification

Spreadsheets and Procedures

Measurement Uncertainty in the Verification of Class I, II, and III Balances

Spreadsheets and Procedures

Measurement Uncertainty in the Verification of Large-Capacity Scales

Spreadsheets and Procedures

Microbiological Method Verification according to ISO 16140-3:2021

Scheduled Courses

e-Learning, In-Person / Streaming

Gain in-depth knowledge of microbiological method validation in your laboratory, applying the latest edition, Part 3 of ISO 16140. This standard represents the cutting edge of the industry and will serve as an essential guide in the near future. With us, you will have the opportunity to explore all the innovations it introduces and learn how to implement them effectively in your laboratory. This course is designed for professionals with prior experience in microbiological method validation. If you want to keep your laboratory up to date with the latest standards and best practices, this is the right place. We will guide you through the key aspects of this critically important standard, enabling you to continue delivering precise and reliable results in microbiological analysis. Get ready to dive into the world of ISO 16140 and learn how to apply it! Access to the platform is 24/7, allowing you to complete the course at your own pace. The course duration is 45 hours and is 100% fundable through FUNDAE.

Microbiological Quality Control

Spreadsheets and Procedures