Escolar Documentos
Profissional Documentos
Cultura Documentos
Release Authorization
Signature
Name: Shri N. K. Subramani
Designation: Dy. General Manager (I/c)
Date: 01/10/2013
Clause
No
Complete Quality
Manual
Page No
Complete Quality
Manual
Complete Quality
Manual
5
6
11
3.4
65
4.1
19
4.2.7
44
Amendment
Reasons
Made
Issue No. 02 brought out to
meet the requirement of
Adequacy report of NABL
Issue No.03 dt.
Issue No. 03 brought out to
09-05-2011
meet the requirement of preassessment report by L.A.
Issue No.04 dt. Laboratory decided to proceed
01-10-2012
for accreditation in calibration
(Mech)
with continual
Audit
01 &
dt. improvement
observation
13-07-13
during
&effectiveness
of management surveillance
audit
system.
Rev: 01 & 23.09.13
Head Office
Audit
(New Delhi)
observation
Issue:04 & 01.10.12 Ensures that the
Audit
integrity of the observation
management
system
01 & Dt.01/10/2013
CalibraCa Calibration lab: Temp.Limit
is 200C 20C, and R.H. is
50 % 20 %. A threshold
noise level is within 60dBA,
and illumination level 450700 lux.
5.3
52
5.6.2.1
01 & Dt.
01/10/2013
Specific
requirement added
for calibration lab.
11
3.4
01 & Dt.
01/10/2013
Date: 01/10/2013
observation
during
NABL Audit
observation
during
NABL Audit
Signature
QM DGM(I/c)
III.
Section
I
II
III
1.0
2.0
3.0
3.1
3.2
3.3
3.4
4.0
4.1
4.2
4.3
4.4
4.5
4.6
4.7
4.8
4.9
4.10
4.11
4.12
4.13
CONTENTS
Contents
Quality Manual Release Authorization
Amendment
Contents
Scope
References
Definitions
Abbreviations
Distribution List
Introduction about the organization
Quality Policy and Objectives
Management Requirements
Organization
Management System
Document Control
Review of requests, tenders and contracts
Sub contracting of tests and calibrations
Purchasing services and supplies
Service to the Customers
Complaints
Control of non conforming testing and
calibration work
Improvement
Corrective Action
Preventive Action
Control of Records
Date: 01/10/2013
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4.14
4.15
Section
5.0
5.1
5.2
5.3
5.4
5.5
5.6
5.7
5.8
5.9
5.10
6.0
7.0
Internal Audits
Management Reviews
Contents
Technical requirements
General
Personnel
Accommodation and environmental
conditions
Test and calibration methods and method
validation
Equipment
Measurement traceability
Sampling
Handling of Test Items
Assuring the quality of test results
Reporting the results
List of System Procedures
Annexure
Date: 01/10/2013
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01/10/13
01/10/13
Rev.No
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Date
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01/10/13
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01/10/13
01/10/13
Date: 01/10/2013
1.0
Scope:
This Quality manual is the apex Quality document of NSICtechnical services Centre, Rajkot, which provides the out line of the
Quality system and defines the Quality policy, objective and scope
of testing and calibration activities. It specifies roles and
responsibilities of personnel concerned with quality, organizational
structure and practices followed by Testing and calibration
laboratories based on ISO/IEC 17025:2005.
The manual guides for activities, methods and procedures followed
in the laboratories as per the international standards and other
relevant specifications as well as specifications given by the
customers.
It covers testing and calibration performed using standard methods
and/or laboratory-developed methods.
It covers the general functioning of the laboratory to improve and
maintain the Management System related to quality in the
laboratory.
Date: 01/10/2013
2.0
References:
General requirements for the competence of testing
calibration laboratories as per ISO/IEC 17025: 2005.
Date: 01/10/2013
and
3.0
Definitions:
Testing: Technical operations that consists of the determination
of one or more characteristics of a given product, process or
service according to a specified procedure
Date: 01/10/2013
which
measures,
III.1
NABL
NSIC
NTSC
DETL
PTL
CSC
BIS
FB
FETL
FHK
FMTL
FQMR
IA
MOU
METL
NC
NCR
OP
P&A
PUR
QM
QMR
SM
SP
PWIM
WIM
WIE
WI
Cal
Cal Lab
Abbreviation:
National Accreditation Board for Testing & Calibration Labs.
National Small Industries Corporation
NSIC Technical Services Centre
Diesel Engine Testing Laboratory
Pump Testing Laboratory
Customer Service Cell
Bureau of Indian Standard
Form / Format / Feed Back
Form / Format of Electrical Testing Lab
Form / Format of House Keeping
Form / Format of Mechanical Testing Lab
Forms/Formats of Quality Management
Internal Audit
Memorandum of Understanding
Mechanical Testing Laboratory
Non Conformity
Non Conformity Report
Operating Procedure
Personnel & Administration
Purchase Department
Quality Manual
Quality Manager
System Manual
System Procedure
Product Work Instruction METL
Work Instruction METL
Work Instruction ETL
Work Instruction
Calibration
Calibration Laboratory
Date: 01/10/2013
3.2
Distribution List
Following are the authorized holders of the controlled copy of the
quality manual.
Controlled Copy
No.
01
02
03
04
05
06
07
08
09
10
Date: 01/10/2013
3.3
Date: 01/10/2013
3.4
Date: 01-10-2013
(Center Head)
Date: 01/10/2013
4. Management Requirements
4.1
Organization
4.1.1
4.1.2
4.1.5 (a)
Date: 01/10/2013
Date: 01/10/2013
4.1.5 (c)
4.1.5(d)
4.1.5 (e)
Organizational Chart
Organization Chart
Laboratory Layout Plan ETL
Laboratory Layout Plan MTL (DETL)
Laboratory Layout Plan Calibration
Date: 01/10/2013
Annexure
Annexure
Annexure
Annexure
3
4
5
6
4.1.5 (f)
The responsibilities, authority and interrelationships of all
personnel who manage ,perform or verify work affecting the quality of
test/calibration are as under roles and responsibilities of Heads.
(f.1) Head of the Centre
Head of the Centre will have overall responsibility to ensure smooth
functioning of all activities of the Centre and take decision for the
same.
Approval of Quality documents and amendments as and when
required before issue.
(f.2)
Quality Manager.
Date: 01/10/2013
(f.3)
Technical manager
(f.4)
Date: 01/10/2013
(f.5)
Maintenance of Equipments.
Planning and Augmentation of facilities in Laboratories.
Upkeep of equipment, sub-systems and environment.
Guidance to the customers for preparation of test samples.
Verification & Signing of test and Calibration reports.
Resolution of customer complaints.
Control of non conforming work and application of corrective
and preventive actions.
Initiations of actions for interlaboratory comparisons.
Head Administration.
4.1.5. (g)
Adequate Supervision.
The respective head will ensure adequate supervision of all
activities taking place in the laboratories. Only competent staff is
allowed to perform the task independently. Other staff may assist.
4.1.5. (h)
Technical Management.
Date: 01/10/2013
Quality Management:
Quality manager is appointed ,who is responsible for development
,implementation ,maintenance and improvement of management
system .he is directly reporting to top management ,where decision
of policy & resources are taken.
4.1.5. (j)
Deputy Assignment.
In the absence of Head of the Laboratory / Quality Manager, Head
of the Centre nominates the replacement time to time.
4.1.5. (k)
Awareness Meeting.
Communication.
4.2
Management System
Date: 01/10/2013
4.2.1.
4.2.2.
4.2.3.
4.2.4.
Quality Policy : Refer Quality Policy and objective at Section No. 3.4
at page no. 11
Evidence of Commitment: The top management reviews the
Management system at regular interval / review meetings
incorporate necessary changes in Management system / provide
replacement of equipment/instruments for quality output.
The top management is committed to meet the importance of
customer requirements as well as Statutory and Regulatory
requirements.
Date: 01/10/2013
4.2.5.
Documentation Structure
Quality Manual
System Manual
Work Instruction
Support Documents
4.2.6
Date: 01/10/2013
4.3.
Document Control:
4.3.1
4.3.1.1.
4.3.1.2
4.3.1.3
Quality Manual
System Manual
4.3.2
4.3.2.1
NABL Publications
ISO/IEC 17025:2005
BIS standards
Date: 01/10/2013
4.3.2.2
(b)
(c)
(d)
for
legal
or
4.3.2.3
4.3.3
Date: 01/10/2013
4.3.3.1
4.3.3.2
4.3.3.3
4.3.3.4.
Date: 01/10/2013
4.4
4.4.1
Review of
Contracts:
Requests,
Tenders
and
Date: 01/10/2013
4.4.3
4.4.4
4.4.5
Date: 01/10/2013
4.5
Date: 01/10/2013
4.6
4.6.1
.
Policy: The laboratory purchases services or supplies of items, form the
competent service provider or supplier, required for testing and
Calibration.
Responsibility: Heads of laboratories and administration.
Procedure: The procedure
NTSC/RAJ/SM/SP/4.3
is
given
in
the
System
Manual
4.6.2.
4.6.3.
4.6.4.
Date: 01/10/2013
testing and Calibration and will maintain records of this evaluation and
list those approved.
Date: 01/10/2013
4.7.
4.7.1
4.7.2
Date: 01/10/2013
4.8
Complaints :
Policy: Complaints and Customer feedback is an important source
of input to enable the laboratory to improve the quality of the
services rendered. Proper redresses of complaint build up
customers confidence in the lab & leads to satisfaction. In lieu of
above, Laboratory accord priority to look into customer complaints
& implement necessary changes to improve the service offered.
Procedure: Procedure for dealing with complaints is given under
System Manual NTSC/RAJ/SM/SP/4.4
Feedbacks from customers are taken by CSC in prescribed
feedback form. Received feedbacks are maintained in CSC.
Any communication from customer in these regards is studied in
detail even if customers statements are biased or unreasonable.
Efforts are made to remove such bias through dialogues and
written communication as the case may be.
A customer complaint / feedback are directly handled by Head of
the Centre and necessary corrective actions initiated.
If complaint points to non-compliance with quality system, that
aspect will be promptly audited & corrective action should be
taken.
If a complaint related to NABL endorsed document is not resolved
within 60 days, NABL should be notified immediately.
Date: 01/10/2013
4.9
4.9.1.
Quality checks.
Internal / external quality audits
Customer complaints / feed back
Routine monitoring / supervision of work
Staff observations
Report / Certificate verification
Calibration of Equipment
Any other such activities
Date: 01/10/2013
Date: 01/10/2013
4.10
Improvement:
The laboratory continuously improves the effectiveness of its management system
through the use of quality policy, quality objectives audits results, analysis data,
corrective action, preventive action and management review.
Date: 01/10/2013
4.11
11.1
Corrective Action
General: A problem with the quality system or with the technical
operations of the laboratory may be identified through a variety of
activities, such as control of nonconforming work, internal or
external audits, management reviews, and feedback from
customers or staff observations. Such problems need to be redress
through corrective actions.
Policy: To provide services of required quality to the customer to
the extent with zero mistakes and to control and prevent recur of
nonconforming work.
Responsibilities: Implementation of corrective actions: Quality
Manager, Technical Manager and Laboratory Incharge.
Monitoring effectiveness of corrective actions: Quality Manager.
Maintenance of records of corrective actions: Quality Manager.
Cause Analysis Team: Quality Manager, Technical Manager and
Laboratory Incharge, Head Customer Service, Customers and / or
external expert (if required)
Suggestion of Corrective Actions: Concerned Laboratory Incharge
and Cause Analysis Team.
Procedure: The procedure for corrective action is given under
System Manual NTSC/RAJ/SM/SP/4.6
4.11.2 Cause Analysis: The cause Analysis Team will investigate for the root
cause(s) of the problem and corrective actions will eliminate the root
cause.
Date: 01/10/2013
and
the
the
the
Date: 01/10/2013
potential
sources
for
the
occurrence
of
Responsibility :
Implementation of preventive actions : Quality Manager,
Technical Manager and Laboratory Incharge
4.12.2
Date: 01/10/2013
Date: 01/10/2013
4.13
Control of Records:
4.13.1
General :
The laboratory has established and maintaining the procedure for
identification, collection, indexing, access, filing, storage,
maintenance and disposal of quality and technical records. Quality
records include reports from internal audits and management
reviews as well as records of corrective and preventive actions.
Policy: Quality records, Technical records and other relevant
records should be easily retrievable on requirement, accessible
only to authorized personnel.
Responsibilities: Laboratory Incharge, Technical Manager/ Quality
Manager.
Procedure: The procedure of identification, collection, indexing,
access, filing, storage, maintenance and disposal of quality and
technical
records
is
given
under
System
Manual
NTSC/RAJ/SM/SP/4.8
The records are legible and stored and retained in such a way that
they are readily identified, retrievable, prevented from damage,
deterioration or loss.
Records are maintained securely for references, audits,
verifications etc. and will not violate the confidentiality policy of the
centre.
4.13.2
Date: 01/10/2013
each Test reports issued are retained for defined period and
indexed as per procedure NTSC/RAJ/SM/SP/4.9.
Observations, data and calculations are recorded at the time they
are taken and are identifiable to the specific task.
On identification of any mistakes in the records are crossed out,
not erased, made neither illegible nor deleted, and the correct
value entered alongside. All such alteration to records are signed or
initialed by the person making correction.
Date: 01/10/2013
4.14.2
4.14.3
The records of the audits like, finding of audits and corrective actions
that arise from that, are maintained by Head of the Laboratory and
put up in Management Review.
Date: 01/10/2013
Date: 01/10/2013
4.14
Management Reviews :
4.15.2
inter-
Date: 01/10/2013
5.0
Technical Requirements:
5.1
General :
5.1.1
5.1.2
Human factors.
Accommodation and environmental conditions.
Test methods and method validation.
Equipment
Measurement traceability.
Samplings.
The handling of test Items.
Date: 01/10/2013
5.2.
Personnel :
Policy: To utilize the capabilities and potential of personnel and
enhance their expertise to undertake present and anticipated tasks
of the laboratory.
5.2.1.
5.2.2.
5.2.3
5.2.4
5.2.5
Date: 01/10/2013
5.3.
Accommodation
Conditions:
and
Environmental
5.3.1.
5.3.2
Date: 01/10/2013
5.3.3
5.3.4
5.3.5.
Date: 01/10/2013
5.4
5.4.1
General: The centre uses appropriate test methods for its operation
within its scope and where appropriate, an expression of
uncertainty as well as statistical techniques for analysis of test and
Calibrationdata.
Procedure includes:
5.4.2
Selection of Methods:
Date: 01/10/2013
5.4.4
Date: 01/10/2013
Validation of Methods :
Validation is the conformation by examination and the provision of
objective evidence that the particular requirements for specific
intended use are fulfilled.
Validation of procedures or methods be carried out by introducing
new test, extension of existing range of operations, software
developed in house, non-standard methods, amplification and
modifications of standard methods to confirm that the methods are
fit for intended use.
Validation satisfies one or more of the following which be finalized
by the validation of methods team.
Comparison of results achieved with other methods.
Inter-laboratory Comparison.
Systematic assessment of the factors influencing the result.
Estimation of uncertainty of the measurements.
Repeatability and reproducibility.
Adequacy of the test or calibration methods and procedures
derived from standard methods.
Validation of software configuration or modification.
For validation of test methods, team be comprised of at least of
Technical Manager, Laboratory Incharge of the concerned
laboratory and Quality Manager.
Date: 01/10/2013
5.4.7
Control of Data :
Calculations and data transfers are subjected to appropriated
checks in a systematic manner.
When computers are used for the processing, recording, reporting,
storage or retrieval of test data, the lab will ensure that :
Computer programme or software is validated as described in the
validation of methods. The commercial off-the-self software ex: MS
Excel, Word processing and statistical programme etc. In general
use within their designated application range may be considered to
be sufficiently validated.
Data such as correction factor; be updated at concerned point of
use safeguarded and secured from unauthorized accesses and
changes.
Date: 01/10/2013
Date: 01/10/2013
5.5.
Equipment :
5.5.1
5.5.2
Equipment and its software used for testing and Calibration are
capable of achieving the accuracy required and comply with the
specifications relevant to test concerned. Equipment used for test
and Calibration is calibrated with valid traceability. Such
Instrument, which do not need calibration but used in test and
Calibration are checked for performance. A list of instrument for
this purpose in each work area identifying the requirement of
calibration, performance check, sources of calibration etc. is made
& quality of equipment is maintained through periodic
calibration / performance check based on planned schedule.
5.5.3
Date: 01/10/2013
5.5.4
5.5.5
5.5.6.
Date: 01/10/2013
5.5.7.
5.5.8.
5.5.9.
When the equipment goes outside the direct control of the lab
(calibration), lab ensure the following :
5.5.10
5.5.11
5.5.12
Date: 01/10/2013
avoid
possible
5.6
Measurement Traceability:
5.6.1
5.6.2
5.6.2.1
Specific Requirements ;
Calibration & Testing:
For testing laboratories, there are some specific requirements
Applied for measuring and test equipments with measuring
functions used, unless it has been established that the associated
contribution from the calibration contributes little to the total
uncertainty of the test result. When this situation arises, the lab
ensures that the equipment used can provide the uncertainty of
measurement needed.
Date: 01/10/2013
5.6.3.
Reference Standards:
5.6.3.1
Reference Standards :
The procedure for maintaining calibration and traceability of
Reference Standards to the National / International standards is
given under System Manual NTSC/RAJ/SM/SP/5.6
5.6.3.2
5.6.3.3
5.6.3.4
Date: 01/10/2013
5.7
Sampling :
5.7.1
Date: 01/10/2013
5.8
5.8.1.
5.8.2
5.8.3
5.8.4
Date: 01/10/2013
5.9
Quality control data is analysed and, where they are found to be outside predefined criteria, planned action be taken to correct the problem and
to prevent incorrect results from being reported.
Such quality-control-check reports are reported to the Head of the
Centre, Laboratory Incharge of Test labs. Analysis of such report
are made by Quality Department and presented by Quality
Manager during Management Review.
Date: 01/10/2013
5.10
5.10.1
5.10.2
Date: 01/10/2013
5.10.3
5.10.4
5.10.5
Date: 01/10/2013
5.10.6
5.10.7
Date: 01/10/2013
6.0
Sl No.
Description
LIST OF SYSTEM PROCEDURE
NTSC/RAJ/SM/SP/4.1
Procedure of Control of Documents
Procedure Review of Requests
NTSC/RAJ/SM/SP/4.2
(Acceptance of Job), Tenders &
Contract
Procedure for Selection of
NTSC/RAJ/SM/SP/4.3
Purchasing Service & Supplies
Procedure for Dealing with
NTSC/RAJ/SM/SP/4.4
Complains
Procedure for Control of NonNTSC/RAJ/SM/SP/4.5
Conforming Testing & Calibration
Work
NTSC/RAJ/SM/SP/4.6
Procedure for Corrective Action
NSIC Technical Services Centre, Rajkot
TITLE :QUALITY MANUAL
Issue No : 04
Revision No 01
Page of
Approved by : DGM
Issued by :
Issue Date: 01/10/2012
Date: 01/10/2013
NTSC/RAJ/SM/SP/4.7
NTSC/RAJ/SM/SP/4.8
NTSC/RAJ/SM/SP/4.9
NTSC/RAJ/SM/SP/4.10
6.0
Sl No
NTSC/RAJ/SM/SP/5.1
NTSC/RAJ/SM/SP/5.2
NTSC/RAJ/SM/SP/5.3
NTSC/RAJ/SM/SP/5.4
NTSC/RAJ/SM/SP/5.5
NTSC/RAJ/SM/SP/5.6
Description
Procedure for training of staff
List of available Formats
Procedure for House Keeping
Procedure
for
Handling,
Transportation, Receipt, Protection,
Storage of Test and/ or Calibration
Items/ Equipments
Procedure
for
Maintaining
Measurement Traceability
Procedure for Maintaining Calibration
& Traceability of Reference Standards
& Materials
Date: 01/10/2013
NTSC/RAJ/SM/SP/5.7
NTSC/RAJ/SM/SP/5.8
NTSC/RAJ/SM/SP/5.9
NTSC/RAJ/SM/SP/5.1
0
NTSC/RAJ/SM/SP/5.1
1
NTSC/RAJ/SM/SP/5.1
2
NTSC/RAJ/SM/SP/5.1
3
NTSC/RAJ/SM/SP/5.1
4
NTSC/RAJ/SM/SP/5.1
5
Date: 01/10/2013
Annexure 1
NTSCRAJ/FQMR/019/FFB/002
7.1
Signature
Date
Quality Manager
Approving Authority
Date: 01/10/2013
7.2
Annexure 2
1.
THE
Date: 01/10/2013
7.2
Standard Specification
1. Induction motors
IS 325 (1996),
IS 7538 (1996)
2. 1Ph Induction motors and Universal motors
IS 996 (1979)
3. Submersible pump set
IS 8034 (1989)
4. Mono set
IS 9079
(1989)
5. Self priming pumps
IS 8418 (1999)
6. Self priming Regenerative pumps
IS 8472 (1998)
7. Open well Submersible pump set
IS 14220 (1994)
8. Submersible motors
IS 9283 (1995)
9. Centrifugal pumps
IS 6595 (2002 )
10. Diesel Monoblock Set
IS 11501
11. Foot Valve
IS 10805
Marking
Terminal Marking
Earthing
Measurement of Stator Resistance
No Load test at Rated Voltage
Reduced voltage Running up test
Full Load test
a. Full load test
b. Duty & Rating
c. Torque
Date: 01/10/2013
Date: 01/10/2013
7.2
Date: 01/10/2013
THE
Quality Manager
Technical
Manager
Incharge
Calibration
Laboratory
Incharge
DIESEL
ENGIE
TESTING
LABORATOR
Y
C.S.C.
Technicians
Date: 01/10/2013
Incharge PUMP
TESTING
LABORATORY
Technicians
Technicians
Date: 01/10/2013
7.4
Annexure 5
MECHANICAL
& CHEMICAL
TEST LAB
NSIC
GODOWN
CALIBRATION
LAB
HOSTEL
MECHANICAL
TEST LAB
DETL
SHEET METAL
WORKSHOP
WOOD WORKING
WORKSHOP
Bhavnagar
Road
ELECTRICAL
TEST LAB
SPTL
OFFICE
MAIN
BLDG
CANT
EEN
GATE
80 Feet Road
Date: 01/10/2013
Annexure 6
BED
No 5
BED
No 6
7.6
BED
No 7
BED
No 4
BED
No 8
BED
No 3
Store Room
WC
DOOR
DOOR
DOOR
BED
No 1
BED
No 10
BED
No 9
BED
No 2
Operator Room
DOOR
DOOR
DOOR
DOOR
Date: 01/10/2013
DOOR DOOR
Office 2
Supervisor Room
Not in Use
Engine
Dimensioning Room
Office 1
Quality Manager
Annexure 7
Lab Eqipment
7.7
V Notch Tank
Door
Pump
Bed
Gauges
Electric
Main
Transformer
Man
Hole
Door
Door
Water Sump
Office 2
NSIC Technical Services Centre, Rajkot
Issue No : 04
Revision No 01
Date: 01/10/2013
Pipe Stand
Annexure 7
A C
aac
A C
Electric Panel
Surface
Plate
GLASS DOOR
Door
MAIN SHUTTER
NSIC Technical Services Centre, Rajkot
Issue No : 04
Revision No 01
Date: 01/10/2013
Date: 01/10/2013