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Tuesday, May 3 2022

Saturday, Jan 1, 2022 midnight
Multi-day Event
Online Courses

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.

Key Session Topics:

  • Definitions
  • Data Integrity and Ethics Regulatory Requirements
  • Improper Practice versus Laboratory Fraud
  • Laboratory Oversight and the Internal Audit
  • Prevention
  • Reporting Issues
  • Laboratory Employee Responsibility

Certificate of Attendance

  • All paid attendees who complete the training and satisfy the course quiz requirements will receive a certificate of attendance

Who Should Attend:

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 Discount:

Group Discounts are available! Contact a Labtopia representative for your unique discount code Group Discount Code Request 

Saturday, Jan 1, 2022 midnight
Multi-day Event
Online Courses

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.

Key Session Topics:

  • Overview of ISO 17025 Standard
  • Understanding the elements of ISO 17025 for technical personnel
  • Maintenance and Calibration Plans
  • Original vs Amended/Corrected Data
  • Amendments and COAs
  • Measurement of uncertainty
  • Decision rule
  • Method validation vs verification
  • Org Chart/ Authorization

 

Assesor Best Practice Advice

Gain insight and best practice advice and tips from a certified ISO 17025 Lead Assessor

Certificate of Attendance

All paid attendees who complete the training and satisfy the course quiz requirements will receive a certificate of attendance.

Who Should Attend

  • Conducting testing or calibration
  • Supporting laboratory activities
  • Managing the laboratory quality system
  • Training laboratory staff
  • Managing the laboratory

 

Course Requirements

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 Discount:

Group Discounts are available! Contact a Labtopia representative for your unique discount code Group Discount Code Request 

 

Saturday, Jan 1, 2022 midnight
Multi-day Event
Online Courses

Online Course - 35 minutes

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.

Key Learning Objectives: 

By the end of this course, you will be able to:

  • Grasp the scope of the administrative and practical requirements associated with ISO 17025 accreditation
  • Form a general impression of the time necessary to achieve accreditation
  • Realize the value of engaging with a consulting partner to help navigate the accreditation journey

Certificate of Attendance

All paid attendees who complete the training will receive a certificate of attendance

Who Should Attend

Anyone interested in understanding the key milestones, required steps and resources, and realistic timeline to implement and achieve ISO 17025 accreditation. 

Saturday, Jan 1, 2022 midnight
Multi-day Event
Online Courses

Three-part online course

  • Part I: Overview – 45 minutes
  • Part II: Lean Tools – 60 minutes
  • Part III: Kaizen/5S Laboratory Application – 55 minutes

 

Course Overview

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.

Key Learning Objectives

By the end of this course, you should be able to:

  • Articulate the importance of efficiency
  • Explain the Lean concept
  • List the tools of Lean manufacturing
  • Identify potential applications of Lean tools in the laboratory
  • Apply Lean manufacturing tools in the laboratory

 

Certificate of Attendance

All paid attendees who complete the training will receive a certificate of attendance

Who Should Attend

Laboratory management, analysts, and laboratory efficiency advocates seeking to improve laboratory productivity, morale, and performance through application of Lean principles.