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Thursday, April 15 2021

Friday, Jan 1, 2021 midnight
Multi-day Event
Online Courses

Online Course - 1.5 Hours

Course Overview:

Enjoy this webinar on your own time at your own pace!

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 registered attendees 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 

 

Friday, Jan 1, 2021 midnight
Multi-day Event
Online Courses

Online Course - 2 Hours

Course Overview:

Enjoy this webinar on your own time at your own pace!

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 Regulator Requirements
  • Improper Practice versus Laboratory Fraud
  • Laboratory Oversight and the Internal Audit
  • Prevention
  • Reporting Issues
  • Laboratory Employee Responsibility

Certificate of Attendance

  • All registered attendees 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 assesor!


Group Discount:

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