Quality System ISO 9001: 2008

The implementation of the system takes place as follows.

Preliminary check up.
Collection from the Company of all the elements necessary for the preparation of an Operational Plan.
Design.
All information gathered during the preliminary check-ups are processed and reported in an Operating Plan.
In the Operational Programme shows the path designed to arrive on schedule for certification.
Development of activities.
The development of the various activities takes place in subsequent stages of implementation developed in meetings in which participate:
The head of the WG,
The employees contemplated in the Project,
The Head of Quality Assurance (RGQ).
Documentation.
The current documentation of the Quality System has identified:
In the Quality Manual, which is the reference document and presentation of the entire Quality System.
In Management Procedures, which are the reference documents for particular activities.
In the Operating Instructions, which are the reference documents to guide operators in their tasks.
In the Forms, which are registration documents of important data for the Quality System and for which it is required their conservation and availability.
Audit.
During the implementation of the Quality System and as planned in the Operational Audit of the Project will be conducted at the Company to verify the implementation, transposition and correct use of all attivtà that have special influence in setting up the system.
Assistance during the certification process.
During its certification ITER, the Leochimica Technical QUALITY 'will follow the Company:
In the Board decision of Certification,
In the preparation of the application for the initiation of the process of certification to be sent to the Institute of Certified chosen,
In the presence as observers during the visit of Certification.

Quality System UNI CEI EN ISO / IEC 17025
The implementation of the system takes place as follows.

Condition assessment.
This first phase involves the collection at the Laboratory Test of all the elements necessary for the preparation of an Operational Plan.
Design
All information gathered during the preliminary check-up will be drawn in the aforementioned document called Operational Project.
The document will address actions to be implemented and in particular:
The different stages of work with the identification of the Working Groups (WG).
The WG will consist of the personnel belonging to the area subjected to the study; they, with the assistance of our. Technicians, will conduct an analysis to streamline the documentation system, informational and organizational flows in respect of that same area.
The duration for the realization of every single phase of work.
Development of activities.
The development of the various activities takes place in subsequent stages of implementation developed in meetings in which participate:
The head of the WG,
The employees contemplated in the Project,
The Head of Quality Assurance (RGQ).
Documentation.
The current documentation of the Quality System has identified:
In the Quality Manual, which is the reference document and presentation of the entire Quality System.
In Management Procedures, which are the reference documents of particular activities and therefore more in-depth and specific activities to which they refer. These documents identify the roles and responsibilities in certain areas of Test Laboratory.
In the Operating Instructions, which are the reference documents to guide operators in their tasks.
In the Test Methods, which are the reference documents for the trial activities.
In the forms, that is, in all of the data recording documents that are important for the quality system and for which it is necessary their conservation and availability.
Audit.
During the implementation of the Quality System and as planned in the Operational Audit of the Project will be conducted at the Laboratory Test to test the implementation, transposition and the proper implementation of the ISO 17025 norm for some activities that are of particular importance in the application of standard itself.
Assistance during the Accreditation process.
During the relative phase of Accreditation ITER, Leochimica QUALITY will follow the Test Laboratory:
In the preparation of the application for the initiation of the process of accreditation to be sent to the Institute of chosen Accreditation and verification of the documentation sent to it.
In the presence as observers during the visit of support to the Accreditation of Testing Laboratory.