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NATIONAL ACCREDITATION
BOARD FOR TESTING AND
CALIBRATION LABORATORIES
(NABL)
What is NABL ?
 NABL specifies the general requirements for the
competence to carry out tests and calibrations,
including sampling. It covers testing and calibration
performed using standard methods, non-standard
methods, and laboratory-developed methods.
Benefits of Accreditation:
 Potential increase in business due to enhanced customer confidence
and satisfaction.
 Savings in terms of time and money due to reduction or elimination
of the need for re-testing .
 Better control of laboratory operations and feedback to laboratories
as to whether they have sound Quality Assurance System and are
technically competent.
 Increase of confidence in Testing / Calibration data and personnel
performing work.
 Customers can search and identify the laboratories accredited by
NABL for their specific requirements from the directory of Accredited
Laboratories.
 Users of accredited laboratories will enjoy greater access for their
products, in both domestic and international markets, when tested
by accredited laboratories.
Types of Laboratory can seek
Accreditation:
 Laboratories undertaking any sort of testing or calibration in
the specified fields.
 Private or government laboratories.
 Small operations to large multi-field laboratories.
 Site facilities, temporary field operations and mobile
laboratories.
TESTING LABORATORIES
CALIBRATION
LABORATORIES
MEDICAL LABORATORIES
 Biological
 Chemical
 Electrical
 Electronics
 Fluid-Flow
 Mechanical
 Non-Destructive Testing
 Photometry
 Radiological
 Thermal
 Forensic
 Electro-Technical
 Mechanical
 Fluid Flow
 Thermal & Optical
 Radiological
 Clinical Biochemistry
 Clinical Pathology
 Haematology &
Immunohaematology
 Microbiology & Serology
 Histopathology
 Cytopathology
 Genetics
 Nuclear Medicine (in-vitro tests
only)
PROFICIENCY TESTING PROVIDERS
REFERENCE MATERIAL
PRODUCERS
 Testing
 Calibration
 Medical
 Inspection
 Chemical Composition
 Biological & Clinical Properties
 Physical Properties
 Engineering Properties
 Miscellaneous Properties
10 Step Approach To Accreditation
 Awareness Training
 Quality Policy & Objectives Finalization
 Gap Analysis
 Documentation / Process Design
 Documentation / Process Implementation
 Internal Audit
 Management Review Meeting
 Shadow Audit
 Corrective –Preventive Actions
 Final Certification Audit
Step 1:- Awareness Training
 Separate training sessions for top management,
middle management and junior level management.
 Creates a motivating environment throughout the
organization for ISO 17025 implementation.
Step 2:-Quality Policy & Objectives
 Work shop with top management on development
of quality policy.
 Work shop with top management and middle level
functional management on development of quality
objectives.
Step 3:-Gap Analysis
 Understanding of all the operations of the
organization.
 Development of process map for the activities of the
organization.
 Comparing existing operations with requirements of
ISO 17025:2005 standard.
Step 4:-Documentation / Process
Design
 Quality Manual
 Functional Procedures
 Work Instructions
 System Procedures
 Formats
Step 5:-Documentation / Process
Implementation
 Work–shop on process / document implementation
as per ISO 17025 requirements.
 Departmental / Individual assistance in
implementing the new processes / documents.
Step 6:-Internal Audit
 Internal Audit Training & Examination (Optional).
 Successful employees / we carry out internal audit
of the organization covering all the departments
and operations.
 Suggest corrective and preventive actions for
improvements in each of the audited departments.
Step 7:-Management Review Meeting
 Quality Policy & Objectives
 Results of internal audit
 Results of supplier evaluation
 Results of customer complaints
 Results of customer feedback etc.
Step 8:-Shadow Audit
 A replica of final certification audit.
 Finds degree of compliance with ISO 17025
standard.
 Gives an idea to the employees about the conduct
of the final certification audit.
Step 9:-Corrective –Preventive Actions
 On the basis of shadow audit conducted in the last
step, all the non-conformities will be assigned
corrective and preventive actions.
 A check will ensure that all the NCs are closed and
the organization is ready for the final certification
audit.
Step 10:-Final Certification Audit
 Upon completion of various stages of accreditation
audit, the audit, your organization will be awarded
accreditation.
THANQ

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NATIONAL ACCREDITATION BOARD FOR TESTING AND CALIBRATION LABORATORI0ES (NABL)

  • 1. NATIONAL ACCREDITATION BOARD FOR TESTING AND CALIBRATION LABORATORIES (NABL)
  • 2. What is NABL ?  NABL specifies the general requirements for the competence to carry out tests and calibrations, including sampling. It covers testing and calibration performed using standard methods, non-standard methods, and laboratory-developed methods.
  • 3. Benefits of Accreditation:  Potential increase in business due to enhanced customer confidence and satisfaction.  Savings in terms of time and money due to reduction or elimination of the need for re-testing .  Better control of laboratory operations and feedback to laboratories as to whether they have sound Quality Assurance System and are technically competent.
  • 4.  Increase of confidence in Testing / Calibration data and personnel performing work.  Customers can search and identify the laboratories accredited by NABL for their specific requirements from the directory of Accredited Laboratories.  Users of accredited laboratories will enjoy greater access for their products, in both domestic and international markets, when tested by accredited laboratories.
  • 5. Types of Laboratory can seek Accreditation:  Laboratories undertaking any sort of testing or calibration in the specified fields.  Private or government laboratories.  Small operations to large multi-field laboratories.  Site facilities, temporary field operations and mobile laboratories.
  • 6. TESTING LABORATORIES CALIBRATION LABORATORIES MEDICAL LABORATORIES  Biological  Chemical  Electrical  Electronics  Fluid-Flow  Mechanical  Non-Destructive Testing  Photometry  Radiological  Thermal  Forensic  Electro-Technical  Mechanical  Fluid Flow  Thermal & Optical  Radiological  Clinical Biochemistry  Clinical Pathology  Haematology & Immunohaematology  Microbiology & Serology  Histopathology  Cytopathology  Genetics  Nuclear Medicine (in-vitro tests only) PROFICIENCY TESTING PROVIDERS REFERENCE MATERIAL PRODUCERS  Testing  Calibration  Medical  Inspection  Chemical Composition  Biological & Clinical Properties  Physical Properties  Engineering Properties  Miscellaneous Properties
  • 7. 10 Step Approach To Accreditation  Awareness Training  Quality Policy & Objectives Finalization  Gap Analysis  Documentation / Process Design  Documentation / Process Implementation  Internal Audit  Management Review Meeting  Shadow Audit  Corrective –Preventive Actions  Final Certification Audit
  • 8. Step 1:- Awareness Training  Separate training sessions for top management, middle management and junior level management.  Creates a motivating environment throughout the organization for ISO 17025 implementation.
  • 9. Step 2:-Quality Policy & Objectives  Work shop with top management on development of quality policy.  Work shop with top management and middle level functional management on development of quality objectives.
  • 10. Step 3:-Gap Analysis  Understanding of all the operations of the organization.  Development of process map for the activities of the organization.  Comparing existing operations with requirements of ISO 17025:2005 standard.
  • 11. Step 4:-Documentation / Process Design  Quality Manual  Functional Procedures  Work Instructions  System Procedures  Formats
  • 12. Step 5:-Documentation / Process Implementation  Work–shop on process / document implementation as per ISO 17025 requirements.  Departmental / Individual assistance in implementing the new processes / documents.
  • 13. Step 6:-Internal Audit  Internal Audit Training & Examination (Optional).  Successful employees / we carry out internal audit of the organization covering all the departments and operations.  Suggest corrective and preventive actions for improvements in each of the audited departments.
  • 14. Step 7:-Management Review Meeting  Quality Policy & Objectives  Results of internal audit  Results of supplier evaluation  Results of customer complaints  Results of customer feedback etc.
  • 15. Step 8:-Shadow Audit  A replica of final certification audit.  Finds degree of compliance with ISO 17025 standard.  Gives an idea to the employees about the conduct of the final certification audit.
  • 16. Step 9:-Corrective –Preventive Actions  On the basis of shadow audit conducted in the last step, all the non-conformities will be assigned corrective and preventive actions.  A check will ensure that all the NCs are closed and the organization is ready for the final certification audit.
  • 17. Step 10:-Final Certification Audit  Upon completion of various stages of accreditation audit, the audit, your organization will be awarded accreditation.
  • 18. THANQ