Defensibility of data is a key issue in the laboratory. Laboratories reporting data for regulatory bodies are required to train employees in data integrity and ethics to ensure that proper laboratory technique is used for generating data. The training will cover common indicators for laboratory fraud and how the supervisor or data reviewer can develop a program to ensure data generated in their laboratory is defensible and complete. An in-depth internal auditing program is important to discover and rectify any evidence of laboratory fraud. Real world examples are discussed to determine if there are any “Red Flags”. Education provides best practices and establishes expectations for the proper method of testing and reporting sample information. This course will address data integrity and ethics in the laboratory as fraud can impact all industries.
This class will meet the requirements for initial and annual employee Data Integrity training for TNI and QSM/DOD.
Pharmaceutical (FDA Regulated Industry), Environmental (TNI and QSM/DOD), Commercial, lab analysts, lab managers, quality managers, and plant managers.
Gain insight and best practice advice and tips from a certified assessor!
Group Discounts are available! Contact a Labtopia representative for your unique discount code Group Discount Code Request
This webinar provides an overview of the ISO/IEC 17025:2017 standard for technical personnel. This course will explain the requirements of ISO 17025:2017 as it applies to their day to day activities. The analyst will gain an understanding of the overall requirements related to all aspects of sample management.
Gain insight and best practice advice and tips from a certified ISO 17025 Lead Assessor
All paid attendees who complete the training and satisfy the course quiz requirements will receive a certificate of attendance.
All attendees are required to own their own copy of the ISO 17025:2017 standard as this course includes items cited directly from the standard. By registering for this course, you agree that you or your company owns a copy of the ISO 17025:2017 standard.
Group Discounts are available! Contact a Labtopia representative for your unique discount code Group Discount Code Request
An invaluable resource when considering ISO 17025 accreditation, this course is designed to provide a step-by-step roadmap for successful implementation. It delivers critical insights for the development of an effective execution plan, outlining what tasks must be accomplished and when. It highlights the resources necessary to navigate the accreditation journey and provides a basis for a realistic, achievable timeline.
By the end of this course, you will be able to:
All paid attendees who complete the training will receive a certificate of attendance
Anyone interested in understanding the key milestones, required steps and resources, and realistic timeline to implement and achieve ISO 17025 accreditation.
Three-part online course
This three-part series provides a thoughtful, reasoned argument for application of Lean principles in the laboratory. Part I provides an overview of the Lean concept and explains how it adds value and eliminates waste. Part II introduces an array of tools and techniques that can be used to implement Lean, and Part III describes how Lean can be applied in a laboratory environment to maximum benefit. Though traditionally employed in manufacturing, this course demonstrates how Lean principles can radically improve efficiency, performance, and morale in the laboratory.
By the end of this course, you should be able to:
All paid attendees who complete the training will receive a certificate of attendance
Laboratory management, analysts, and laboratory efficiency advocates seeking to improve laboratory productivity, morale, and performance through application of Lean principles.
Four-part online course
This four-part series provides a foundational understanding of quality management and its integral role in the functions of an efficient, well-run laboratory. Part I defines quality management and describes its benefits. Documents and records – the pillars of an effective QMS – are examined in Part II. Part III addresses nonconforming work and deviations, offering insight on how both should be addressed. Finally, Part IV differentiates between corrective and preventive action, placing each in context with regard to the QMS.
By the end of this course, you should be able to:
All paid attendees who complete the training will receive a certificate of attendance
Technical personnel new to quality management systems, new quality team members, and anyone interested in understanding the building blocks of quality management and requiring an understanding of quality management systems as applied in the laboratory.