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NATIONAL ACCREDITATION
NABL
BOARD FOR TESTING AND
CALIBRATION LABORATORIES
PRE-ASSESSMENT
GUIDELINES AND FORMS
ISSUE NO : 02 AMENDMENT NO : 00
ISSUE DATE: 01.03.2008 AMENDMENT DATE: --
AMENDMENT SHEET
10
Amendment Sheet i
Content ii
1. Introduction
It is presumed that the Lead Assessor who has been nominated by the NABL
Secretariat, is fully aware of the NABL Accreditation process, its objectives and the on-
site Assessment procedure. The Lead Assessor shall have the overall responsibility of
conducting the assessment and shall be responsible for evaluating the adequacy of
the Quality Manual, pre-assessment of the laboratory and for conducting the on-site
assessment of the concerned laboratory. Towards the task of on-site assessment, he
shall be assisted by a team of assessors commensurate with the scope of
accreditation.
This document contains Pre-assessment form and Checklist, which will form a part of
the Pre-assessment Report. The document shall guide the Lead Assessor in
completing various forms & checklists and compiling the report.
2. Pre-Assessment
After the laboratory has taken the corrective action on the concerns expressed in the
adequacy report and has submitted a report to the satisfaction of the NABL & Lead
Assessor, NABL Secretariat shall fix up a date for Pre-assessment in consultation with
the laboratory and the Lead Assessor.
While the Lead Assessor proceeds to the laboratory for Pre-assessment, he should be
in possession of the laboratory’s Applications Forms, Quality Manual, Corrective action
report on the adequacy of the Quality Manual and any other information supplied by
NABL Secretariat.
i. check the implementation of the Quality System as per the documented Quality
Manual
ii. study the scope of accreditation so that the time frame, number of assessors
required in various fields and visits to Site testing/ calibration facilities, if
applicable, for the assessment can be determined. The Lead Assessor shall
also assess whether the Assessment is required to be split, based on the
location of laboratory or the number of fields/ departments.
iii. check whether the laboratory has conducted a comprehensive Internal Audit in
accordance with ISO/ IEC 17025: 2005 or ISO 15189: 2007 which ever is
applicable.
iv. assess the degree of preparedness of the laboratory for the Assessment in
terms of compliance to NPF 1.
The Lead Assessor must review the Laboratory’s documented Quality System to verify
compliance with the requirements of ISO/ IEC 17025: 2005 or ISO 15189: 2007 which
ever is applicable. He should complete the Checklist NPF 1 by recording his
observation – ‘Yes’ or ‘No’ (by marking a in the appropriate box), related to the
requirements of respective clause number of the checklist and offering brief
comments. If the Lead Assessor has a doubt in other area(s), not listed in the
checklist, he is free to assess or go into details where he feels and annex his findings,
to the report.
The Lead Assessor shall submit the Pre-Assessment Report to NABL Secretariat
within 10 days of completion of Pre-Assessment.
4. Internal Audit
Availability of Audit Procedure
Availability of Audit Plan
All requirements of ISO/ IEC 17025: 2005 or ISO 15189: 2007
which ever is applicable, covering all activities of laboratory
audited at least once in the last one year
Timely corrective action on non-conformities
Audit conducted by Independent and competent personnel
Comments on effectiveness of Internal Audit:
5. Management Review
Availability of Management review Procedure
All requirements of ISO/ IEC 17025: 2005 or ISO 15189: 2007
which ever is applicable, are incorporated in the agenda of review
in the last one year
Evidence of at least one review
Comments on effectiveness of review:
6. Personnel
Training programme on ISO/ IEC 17025: 2005 or ISO 15189:
2007 which ever is applicable, organised for laboratory personnel
Plan/ Schedule for imparting training to laboratory personnel for
the current year
Suitability of persons authorised to sign test/ calibration reports
with reference to the field(s) applied
Comments on Personnel and Training:
Signature/ Name of Authorised Personnel of Lab. & Date Signature/ Name of Lead Assessor & Date
Note: Use additional sheets of this form, if required
PRE-ASSESSMENT REPORT
Laboratory:
Quality Manager: Date(s) of Visit:
Facility: Testing/ Calibration/ Medical Field(s):
Applicable Standard: ISO/ IEC 17025: 2005 ISO 15189: 2007
Persons Contacted:
Signature/ Name of Authorised Personnel of Lab. & Date Signature/ Name of Lead Assessor & Date