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