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Perry Johnson Laboratory Accreditation Inc.
United States
Registrace 9. 10. 2012
Perry Johnson Laboratory Accreditation, Inc. (PJLA) is a private organization, offering third-party accreditation services for testing and calibration laboratories. We are absolutely committed to meeting and exceeding the requirements and expectations of our clients in terms of the quality of the services we provide. We are a fully recognized accreditation body by the International Laboratory Accreditation Cooperation (ILAC) and by the Asia Pacific Laboratory Accreditation Cooperation (APLAC) to provide testing and calibration accreditation services.
755 W Big Beaver Rd, Ste 1325
Troy, Michigan 48084
(248) 519-2603
755 W Big Beaver Rd, Ste 1325
Troy, Michigan 48084
(248) 519-2603
A Summary of Changes of the DoD/DOE ELAP QSM Version 6.0 and PJLA Transition Requirements
Join PJLA for an informative webinar detailing the latest updates in the Department of Defense (DoD) and Department of Energy (DOE) Environmental Laboratory Accreditation Program (ELAP) Quality Systems Manual (QSM) Version 6.0. This session will cover essential changes and the necessary steps for transitioning to the new requirements. Don't miss this opportunity to stay ahead of the curve and ensure your laboratory's compliance.
Key Takeaways:
- Overview of the major changes in QSM Version 6.0
- Understanding the impact of these changes on your laboratory operations
- Detailed transition requirements and timelines from PJLA
Register now to secure your spot and keep your laboratory accredited and compliant with the latest standards.
Presented by: Matthew Sica, Technical Program Manager, Perry Johnson Laboratory Accreditation, Inc. (PJLA)
Key Takeaways:
- Overview of the major changes in QSM Version 6.0
- Understanding the impact of these changes on your laboratory operations
- Detailed transition requirements and timelines from PJLA
Register now to secure your spot and keep your laboratory accredited and compliant with the latest standards.
Presented by: Matthew Sica, Technical Program Manager, Perry Johnson Laboratory Accreditation, Inc. (PJLA)
zhlédnutí: 48
Video
AOAC Hemp & Cannabis Proficiency Testing - A Solution to a Critical Need
zhlédnutí 69Před 2 měsíci
Hemp and cannabis testing laboratories are evolving swiftly. New and diverse analytical methodologies are continuously being developed to address the needs of the rapidly growing cannabis and hemp industry, and the changing regulatory landscape surrounding these materials. Whether the focus is on ensuring products are free of dangerous pesticides, heavy metals, or microbials, or on characterizi...
PJLA with CannabisTalk101 - What is PJLA?
zhlédnutí 17Před 2 měsíci
Tracy Szerszen is featured on Cannabis Talk 101 to explain what PJLA does and how our company fits in the cannabis labs regulatory space. For more information on how to get accredited give us a call at 1-877-369-5227, or visit our website at PJLabs.com
FDA Laboratory Accreditation for Analyses of Food (LAAF) Program -Lessons Learned
zhlédnutí 139Před 3 měsíci
Gain a comprehensive understanding of the expectations set forth by the FDA LAAF program and learn practical techniques for effectively navigating the accreditation process. Elevate your knowledge and readiness for accreditation by joining us for this essential session. Presented by Leeza Akimenko, PJLA Lead Assessor/ Food Testing Program Advisor
A Look at ISO/IEC 17025:2017 - Requirements Concerning Impartiality and Confidentiality
zhlédnutí 446Před 3 měsíci
Impartiality can be defined as “the presence of objectivity.” Confidentiality can be defined as “the state of keeping or being kept secret or private." The first two sections of ISO/IEC 17025:2017 takes into the requirements of both impartiality and confidentiality. This webinar will look at these requirements and will clarify what they are and how an organization can comply with meeting these ...
A Look at the ISO/IEC 17025:2017 - Requirements Concerning Document Control and Control of Records
zhlédnutí 454Před 4 měsíci
ISO/IEC 17025:2017 requires all laboratories to control all documents which include both internal and external documents. The realm of what is considered a document will be discussed. This webinar will look at these requirements and provide detail as to what they mean. Control of records are broken into technical and quality related records. The webinar will look at what constitutes a record an...
Measurement Uncertainty and Decision Rules with Dr. Susan Audino
zhlédnutí 617Před 5 měsíci
No measurements are without error or uncertainty and each answers a different question. This session will focus on measurement uncertainty and its critical role in decision rules when making statements of conformity to predefined specifications or criteria. We will disentangle measurement bias from measurement uncertainty, discuss how and when to determine uncertainty, and finally understand it...
Common Findings in Assessments to the ISO/IEC 17025:2017 Standard in 2023
zhlédnutí 654Před 6 měsíci
We have looked back at assessment done by PJLA during the 2023 calendar year and have compiled data from these assessments. This webinar will look at the area’s which were identified as the top list of nonconformance’s which PJLA assessors wrote during the year. We have identified some reoccurring issues found during PJLA assessments during 2023. This webinar will look at some common findings f...
The 5 Step Laboratory Accreditation Journey - with PJLA
zhlédnutí 212Před 6 měsíci
In this video, we guide you through the five essential steps to achieve laboratory accreditation, ensuring precision, reliability, and compliance in your testing processes. Join us on the five step journey of quality assurance and discover the keys to maintaining high standards in your laboratory operations. For more information, visit our website at www.pjlabs.com/ or call us at 1-877-369-5227
Adding DOECAP-AP Accreditation to a DoD ELAP Accredited Laboratory
zhlédnutí 96Před 7 měsíci
Did you know that almost one-half of the DOE Consolidated Audit Program - Accreditation Program (DOECAP-AP) laboratories perform routine and project specific non-radiological analysis? There are opportunities for non-radiochemistry laboratories to support projects involving routine compliance monitoring, site characterization, process control testing, and remediation for various environmental m...
Things to Consider When Choosing an Accreditation Body - Highlight
zhlédnutí 47Před 7 měsíci
Choosing the right accreditation body is crucial for your business's success. Discover why Perry Johnson is the top choice! 🚀 🤝 Benefit from a Dedicated Support Team: Our experts are committed to guiding you through the accreditation process, ensuring a seamless experience from start to finish. 📞 Prompt & Professional Communication: Experience clear and timely communication with our team, addre...
Why Accreditation? The Key Advantages of Accreditation - Perry Johnson Laboratory Accreditation
zhlédnutí 718Před 8 měsíci
Why should I become accredited? Accreditation provides the marketplace confidence that your organization has a well-established quality management system producing reliable and accurate results. Accreditation is utilized globally by various industries to confirm traceability in results. Becoming accredited symbolizes integrity and competency within your organization which provides you a market ...
A Look at ISO/IEC 17025:2017 - Section 6.6 - Externally Provided Products and Services
zhlédnutí 312Před 8 měsíci
When you are selecting a potential vendor, you are selecting a partner in your business which you will trust to work with you in a professional and profitable manner. It is important that you choose a company that can supply your current and future needs. Section 6.6 combines both purchasing and subcontracting. This webinar will take a look at requirements for retaining records and having proce...
Understanding the PJLA Flexible Scope Policy for Testing Labs, RMPS, and PTPs
zhlédnutí 133Před 9 měsíci
Understanding the PJLA Flexible Scope Policy for Testing Labs, RMPS, and PTPs
PJLA attends the Automotive Testing Conference 2023, Novi, Michigan
zhlédnutí 73Před 9 měsíci
PJLA attends the Automotive Testing Conference 2023, Novi, Michigan
A Look at ISO/IEC 17025:2017 - Overview of the Requirements Specified for Equipment in Section 6.4
zhlédnutí 490Před 9 měsíci
A Look at ISO/IEC 17025:2017 - Overview of the Requirements Specified for Equipment in Section 6.4
Introducing the PJLA Referral Program
zhlédnutí 3,5KPřed 10 měsíci
Introducing the PJLA Referral Program
Measurements Gone Wrong Webinar with PJLA & Henry Zumbrun
zhlédnutí 188Před 10 měsíci
Measurements Gone Wrong Webinar with PJLA & Henry Zumbrun
A Look at ISO/IEC 17025:2017 - Requirements for Corrective Action
zhlédnutí 666Před 11 měsíci
A Look at ISO/IEC 17025:2017 - Requirements for Corrective Action
An Overview of 17043 Proficiency Testing Provider Accreditation with PJLA
zhlédnutí 975Před rokem
An Overview of 17043 Proficiency Testing Provider Accreditation with PJLA
A Review of the Revised PJLA Policy PL-4 “Scopes of Accreditation”
zhlédnutí 244Před rokem
A Review of the Revised PJLA Policy PL-4 “Scopes of Accreditation”
Understanding the Types of Reference Materials, Their Differences, and Their Uses
zhlédnutí 841Před rokem
Understanding the Types of Reference Materials, Their Differences, and Their Uses
I Submitted a Complaint - Why is this Organization Still Accredited?
zhlédnutí 170Před rokem
I Submitted a Complaint - Why is this Organization Still Accredited?
Use of Accreditation Symbols and References to Accreditation
zhlédnutí 125Před rokem
Use of Accreditation Symbols and References to Accreditation
A look at ISO/IEC 17025:2017 - Section 7.2 “Selection, Verification, and Validation of Methods"
zhlédnutí 1,4KPřed rokem
A look at ISO/IEC 17025:2017 - Section 7.2 “Selection, Verification, and Validation of Methods"
A Look at ISO/IEC 17025:2017 - Review of Section 8.5 “Actions to Address Risks and Opportunities”
zhlédnutí 1KPřed rokem
A Look at ISO/IEC 17025:2017 - Review of Section 8.5 “Actions to Address Risks and Opportunities”
A Look at ISO/IEC 17025:2017 - Section 7.6 “Evaluation of Measurement Uncertainty” for Testing Labs
zhlédnutí 1,9KPřed rokem
A Look at ISO/IEC 17025:2017 - Section 7.6 “Evaluation of Measurement Uncertainty” for Testing Labs
Common Findings in Assessments to the ISO/IEC 17025:2017 Standard in 2022
zhlédnutí 2KPřed rokem
Common Findings in Assessments to the ISO/IEC 17025:2017 Standard in 2022
That was fast 😂
This training is very interesting for proficiency testing provider
Very good
Very Good Information
Thank you
Informative❤
Clause 8.9 does not require a meeting.
Thank you for sharing,
Thank you for sharing,
This is very important topic for us ASINAL laboratory - Bogota, COLOMBIA
I found it informative and enjoyable! The list of references is particularly appreciated.
31:57 it's insane how many scammy "consultants" exist in the cannabis industry. They are awful especially when lab owners dont understand sound scientific principles and trust the consultants over their own analysts!
26:22 no personal opinions, everything is based on the results conducted and following clearly defined methods and procedures. This is crucial.
Thank you, very informative webinar.
Dear Sir, Under "Good Practice for Internal Auditing" slide, you have mentioned the audit criteria as quality management system documents only and not the ISO/IEC 17025-2017 standard. Then the deficiencies of adequacy of quality system documentations with the ISO/IEC 17025-2017 standard can not be detected in internal audit. To my mind most of the deficiencies (NCs) has a root cause related to system documents, or in other way, it is found that the effective corrective action for NCs always leads to changes in system documents, for sustenance. Therefore, is taking system documentation as criteria, good practice enough compared to taking the audit criteria as ISO/IEC 17025-2017 standard and applicable policy and requirement documents of the accreditation agency. Besrt regard. Subhaiss Mallik, Assessor in ISO/IEC 17025-2017. Thanks in advance for your kind advice.
Love your presentations PJLA - the best I've seen so far!!!
How do you know when to stop asking 'Why'?
Hey! Thanks for your comment. For more information, feel free to email pjlabs@pjlabs.com and they will point you in the right direction.
Hi, What is a method deviation? how the personel can identify method desviations?
Hello! Feel free to reach out to pjlabs@pjlabs.com for help with any questions.
What does type identification from clause 6.4.13 mean?
Реально классный канал
Отлично
😮
My main takeaway was that the process is difficult, and ultimately relies on the testing lab honestly&completely reporting&validating their errors and corrective actions. One super easy and free option you have for validating test labs is asking for a copy of their most recent Proficiency Test Results. These proficiency tests are blind (the lab doesn't know the answer while doing the analysis) and are mostly ran by reputable agencies. It might be a good idea for ISO accreditation agencies to build a prearranged "complaint handling fee" into their service agreements. Perhaps they do? At least then they get paid something for the time they're spending investigating complaints. The added cost would also encourage labs to do things right and make use of their internal complaint handling system so that complaints don't have to be elevated to their accreditation agency. A downside would be potential abuse of the complaint reporting system, but there are ways to tell if a complaint is legitimate (ask for data).
Exceptional webinar! PJLA is doing an awesome job. I really appreciate your efforts. Main concepts about bias, random and systematic effects are discussed in this webinar.
What would be the action plan for opportunities and how to make all these points in opportunities. Also is there any sop we need to made for this
Good stuff Thank you Sir
Greetings! I'm having difficulty in understanding the clause 7.10.1 b. I'm trying to set risk levels in the procedure but how can I set a criteria for those levels and the actions. I'm confused and stuck at this point. Need your response it.
Kindly help for uncertainty applied for pharmaceutical RnD
Hello, i have just started a job in a materials lab (concrete, aggregates, etc...). I was assigned to check a bunch of astm materials tests' uncertainty. Would you allow me to reach out by any social media contact info? I got questions about this stuff even though it's beyond my expertise!
Hello - please feel free to reach out to PJLA HQ at www.pjlabs.com/contact-us or call 1-877-369-5227 and they will direct you to someone who can answer your questions.
Hi sir! please answer how do you ensure impartiality & confidentiality in case of in-house testing facility? at what point in an organizational structure the head can be same as that of production? Does the lab need a separate independent identity for accreditation?
Hello Ankita - please feel free to reach out to PJLA HQ at www.pjlabs.com/contact-us or call 1-877-369-5227 and they will direct you to someone who can answer your question.
It will affect impartiality ,need to make separate organogram .it need to address 4.1.5 of your quality manual
I hate Iso
PJLA have online training ISO/IEC 17025:2017 or not ? I want to learn and download documents like this video.
Laboratory
I am new subscriber. I will follow you with ISO/IEC 17025.
Thank you very much.
Thank you for training online. Point 7.6 and 7.7 is very interesting for laboratory.
good video
Thanks for making this video,very informative
Great to hear long time ))))
Dear sir I not understand what you mean objective evidence that internal audit in 7/12/2021 not recorded ??? You mean that the lab not complete the all interval plan within the year ???
Hello! Please feel free to email pjlabs@pjlabs.com with any questions ✅
Great content 👍 ThX for the good work
Lab Services Standardization and Quality Management System
No
Laboratory
Good discussion breaking down rapid (PCR) vs traditional culture methods for product release.
Thank you for this informative session. Please i need help , i am looking to build/complete the 17020 : 2012 checklist for a small start up IT Services Consulting Firm and want to ask if you have any guide or extract on the list of documents to be generated internally. The checklist is too broad and may not directly apply to my industry, making it hard to figure which requirements are mandatory or which could be grouped together and fulfilled by one document. Thank you.
one of the best webinars on measurement uncertainty and validity of results
So, should this "lab management" be a single person or it can be a team consisting of "quality manager" and "technical manager"?
Good stuff presented. Thank you sir
Thank you