Learn about ISO/IEC 17025 standard for testing and calibration laboratory management system and standard requirement of ISO/IEC 17025 certification. This presentation cove what is accreditation, benefits, documentation and more.
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What is ISO/IEC 17025?
The ISO 17025 standard specifies the general requirement for the ability
to hold out tests and calibration as well as sampling. The check and
calibration ways performed area unit categorized as standard, non-
standard and laboratory developed. It covers 1st, second and third party
laboratories wherever testing and calibration forms a part of scrutiny and
products certification. This international ISO 17025 standard is
applicable to all or any laboratories in spite of the amount of personnel
or the extend of the scope of testing and calibration activities. it's
employed by laboratories to develop their management system for
quality, body and technical operations.
3. What is Accreditation?
Accreditation could be a formal, third party recognition of competency
to perform specific tasks. It provides a method to spot a established,
competent authority so the choice of a laboratory, review or certification
body is associate enlightened alternative. ISO 17025 accreditation
suggests that the authority will demonstrate to its client that it's been
winning at meeting the wants of international accreditation standards.
Usually the explanation for obtaining one thing severally evaluated is to
verify it meets specific needs so as to scale back risks. Obvious
examples are product failure, health risks, company name or to satisfy
legal or client needs. something or anyone is evaluated - product,
equipment, people, management systems or organizations.
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4. Aim of ISO/IEC 17025
Provide a basis for use by accreditation bodies in assessing the
competence of laboratories.
Establish general requirements for demonstrating lab compliance to
perform specific tests or calibrations.
Assist in the development and implementation of a lab's quality
system.
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6. Elements of ISO/IEC 17025
Scope: The area of the lab being evaluated that will represent the lab
as a whole (i.e. mechanical equipment, environmental conditions)
Normative References: Documents that give the most recent
information about every area of the process and equipment standards.
Terms and Definitions: The labeling of all equipment, instruments,
work stations, employees, and defining instructions, protocol, procedure,
and safety measures.
Management Requirements: document control, service to clients,
contract reviews, preventative actions, internal audits, management
reviews, etc.
Technical Requirements: Safe working conditions, functional
equipment, proper calibration of devices, handling of tests and
substances, result reporting etc.
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7. What is ISO/IEC 17025 Management Requirements
Organization
Management System
Document control
Review of requests, tenders and contracts
Subcontracting of tests and calibrations
Purchasing services and supplies
Service to Customer
Complaints
Control of non-conforming testing/ calibration
Improvement
Corrective actions
Preventive actions
Control of records
Internal audits
Management reviews
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8. Benefits of ISO/IEC 17025
Increase in productivity
Rework and retesting reduction
Reduced instrument repairs and defect levels
Due to establishment of control chart and regular monitoring test and
instrument capability is improved in turn benefited in Higher yield
Improvement in knowledge level and multi skirling
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9. What to Document for ISO/IEC 17025
Accreditation
ISO/IEC 17025 documents used to designed
and developing testing and calibration
laboratory. The laboratory management system
needs standard documents that cover all
requirements of ISO/IEC 17025:2005 for quick
accreditation. Following are the key document
provided by ISO 17025 consultant.
Manual
Procedures
Standard Operating Procedures
Exhibits
Blank and Filled forms
Audit checklist
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