This ISO/IEC 17025:2017 Implementation Workshop uses practical examples to help participants understand how to implement various aspects of a laboratory management system
$977.00
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16 hours
Combination lecture and classroom exercises
Available at QSG’s training facilities, on-site at your organization, and virtually
Start date: November 25, 2024
End date: November 26, 2024
Start time: 08:30 a.m. EDT
End time: 04:30 p.m. EDT
Venue: Virtual on Zoom
Directions: Training located at Quality Support Group, 319 Littleton Rd STE 206, Westford, MA 01886. Please plan to arrive 15 minutes prior to the training session start time.
ISO/IEC 17025 specifies the general requirements for the competence to conduct tests and/or calibrations, including sampling. It covers testing and calibration quality systems using standard methods, non-standard methods, and laboratory-developed methods.
ISO/IEC 17025:2017 consists of five elements: Scope, Normative References, Terms and Definitions, Management Requirements, and Technical Requirements. The two main sections are Management Requirements and Technical Requirements. Management Requirements are primarily related to the operation and effectiveness of the laboratory’s quality management system. Technical Requirements includes factors that determine the correctness and reliability of the tests and calibrations performed by the laboratory.
This ISO/IEC 17025:2017 Implementation Workshop uses practical examples to help participants understand how to implement various aspects of a laboratory management system, and includes training on:
This course is designed for:
Food, environmental, chemical, and clinical testing laboratory personnel
QA managers and personnel
Analysts and lab managers
Training department personnel
Documentation department personnel
Consultants
Through training, participants will learn:
The key clauses of ISO 17025
The laboratory accreditation process, including the benefits and considerations
How to develop a plan for implementing ISO 17025
What is required for the maintenance of an ISO 17025 system
Day 1
On Day 1 of this training course participants will learn about the fundamentals of ISO17025, including exploring the relationship between ISO 17025 and other standards, and the difference between Certification and Accreditation, including analysis of the benefits and considerations of these options.
Day 2
On Day 2 participants will explore ISO 17025 management system requirements and develop implementation skills, including performing a gap analysis, creating high level process maps, understanding risks and opportunities of implementation, and developing an implementation plan.
Bob,
Thank you for all of your time and assistance with both; the Internal Audits and the Gap Analysis. I strongly feel that our QMS will have great improvements from these events.
Hi Bob,
Not sure if I ever told you, but the quality manual spreadsheets you provided have impressed every external auditor that’s come in.
We are grateful to you for sharing the template with us. We were certified to the 2015 version of the standard in December and the auditor said we saved him hours of auditing because we had all the information in one place.
More recently a customer asked if we might share the template with them. But I wanted to ask you if that would be alright before doing so.
Please let me know as soon as you can. Take care.
Hi Al,
I want to tell you how pleased everyone was with how far we have come. That is due in no small part to your efforts and coaching. Scott and I appreciate what you have done.
We had our ISO 9001:2015 certification audit this week and we passed with flying colors! No findings and only 3 OFI’s. We should be receiving our certificate in 4-6 weeks.
I wanted to say Thank You, to you and the QSG team for helping us with this transition. Your assistance certainly made it a much less daunting of a task for us to achieve. I’ll be sure to contact you when it’s time for our internal audit.
Thanks again for all your help!
Angelo,
It feels nice to put the successful audit behind us! We filed our corrective action report and sent it over last Friday. We should get our official re-certification in the coming days.
Al was a great resource in pulling us through this project. He fit well with the team. With Al and Don, you have some quality people working for your organization.
We’ll be getting back in touch with Al next month to begin scheduling out the training for ISO 9001:2015.
To Bob, Angelo, and Al,
As you have heard we successfully completed our ISO 9001, 2015 audit this past week with no findings and only 2 observations for improvements. I would like to thank you all for your efforts in helping us complete our journey. I’m confident this will make Vacuum Barrier a stronger organization going further. We will keep you in mind as additional demands surface that we may require your services again.
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