Real Life Laboratory Experience and ISO 17025 consultancy

Who We Are?

CAL LAB ACCESS, LLCis an organization founded in the year 1995. CLA is a global team of quality and technical professionals with a combined world experience of more than 25 years. We (CLA) are in business to help calibration laboratories to improve business, customer relations, expand calibration capabilities, lean process, quality management system and training documentation (technical & quality) based on national & international standards. Please visit our newly designed website (www.callabaccess.com).

Feel Free to Consult Real life laboratory experience

ISO/IEC 17025 Highlights:

Three other important things that you will be hearing about as you move forward with this project….

1. Process Approach –

Application of a system of Processes and their Interactions

Laboratory Quality Management System (LQMS) will incorporate the process approach where consistent and predictable results are achieved more effectively and efficiently when activities are understood and managed as interrelated processes.

ISO/IEC 17025uses a process approach where a process is an action that turns inputs into outputs, like turning ice to water by heating it.So,as we (CLA) look at your business as a series of interacting processes, we (CLA)can try to improve them for better resultsno matter what the process is in your laboratory.

Identifying, understanding and managing interrelated processes as a 

system helps your company effectively and efficiently achieve yourlaboratory objectives. 

                             

 

2. Plan-Do-Check-Act –A Cycle for Continual Improvement

The Plan-Do-Check-Act approach requires that we (CLA) create and implement a plan to achieve the desired results. This is true for any type of management system and it is simply good business practice. ISO standards use this PDCA approach in all their Management Systems because it is really just a way to get things done and continually improve.

                                                          

Cal Lab access offers best ISO 17025 consultancy for Laboratories.

3. Risk-Based-Thinking

A proactive approach aimed at preventing undesirable outcomes

We (CLA)will make use of your organizational knowledge, lessons learned and experience withyour activities and the processes to determine the opportunities and risk that need to be addressed.

This way, we (CLA) will have assurance that we can achieve the intended objectives of producing accurate and valid results and eliminating errors.

                                                        

Why you required ISO 17025 Consultants Help?

Introducing Quality Policy

Top Management will develop a Quality Policy to demonstrate their commitment and leadership with respect to the Laboratory Quality Management System. How does your work contribute to meeting company’s Quality policy?

Each and every individual has an impact on the performance of the laboratory.

How Our ISO 17025 consultancy Can Helpful for you?

We have a complete team of ISO 17025 consultants who will help in implementing and effective laboratory management system in compliance with and complete the process to get certified ISO 17025. 

     

Who We Are?

CAL LAB ACCESS, LLC is an organization founded in the year 1995. CLA is a global team of quality and technical professionals with a combined world experience of more than 25 years. 

Step 1: Gap Analysis

The next step in getting the Laboratory Quality Management System (LQMS) accredited to ISO/IEC 17025:2017 is to conduct a “Gap Analysis”.

This is an evaluation of current processes to see what you have in place that already meets the requirements of ISO/IEC 17025:2017, and what you will need to do to meet the remainingrequirements.

In most cases, your company’s quality department or a consulting firm such as CAL LAB ACCESS will come to all departments and asking how you do things. They will want to see procedures and records, so they can evaluate the current method of doing things against the requirements of the standard. This information will help them plan ISO/IEC 17025:2017 Project.

After the Gap Analysis…

When we (CLA) have completed the Gap Analysis, your quality team and CLA will put together a plan to address the requirements of the ISO/IEC 17025:2017standard. This plan will include outlining new ways of doing things and developing documented information for the laboratory processes.

Many employees will be involved in this effort.CLA and quality teams will be documenting and updating the way of doing things in Procedures and Work Instructions.

 

ISO/IEC 17025 Highlights: Things that you will be hearing as your company proceed with this project….

Documented Information

Documented information will support the operation of your activities and the processes and will provide confidence that they are carried out as planned.

Procedures will be written to describe how a process or activity is done. For example, a procedure for the Control of documented information is written to describe the overall document control process. When detailed instructions are needed, a work instruction will be written to describe how to do a task or process. In the example above, a procedure is written describing the overall control process. A work instruction is written to describe how to assign control numbers forthe documents.

Other Blog - What is ISO/IEC 17025:2017?