KSPH&IDCL IMS Procedure IMSP 01

Control of Documents

1.0 Purpose
The purpose of this procedure is to define controls needed for the documents of integrated
management system (QMS+EMS). Records are a special type of document and are
controlled as per IMSP 02.

1.1 Application
This procedure is applicable to all documents concerned with IMS including documents of
external origin such as National / International standards and customer supplied documents.

2.0 Responsibility
Responsibility and Authority for various activities of ‘Document control’ is described in
procedure part.

3.0 Terms and definitions

a) Document: Information and its supporting medium. A set of documents, for example
specifications and records, is frequently called documentation.
b) Form: Document used to record data required by the IMS management system
Note: A Form becomes a record when data is entered.
c) Record: Document stating results achieved or providing evidence of activity performed

4.0 Abbreviations
IMS = Integrated Management System
IMSM = Integrated Management System Manual
IMSP = IMS Procedure
WI = Work Instruction
CL = Checklist
ASL = Approved supplier list
ML = Master list
F = Form
AP = Audit plan
QP = IMS Plan

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Control of Documents

5.0 Procedures

5.1 Document preparation guide

Where and to the extent possible, guidelines given in the following standards should be
adapted:
1) ISO/TR 10013:2001 – Guidelines for IMS management system documentation
2) ISO 10005:1995 – Guidelines for preparation of IMS plan
While developing Forms, following issues to be considered as appropriate:
a) Customer requirements
b) User requirements
c) M.I.S requirements
d) Statutory and regulatory requirements

5.2 Documentation structure and numbering system

Document description Numbering system

Level 1 Document IMSM XX

IMSM = IMS Manual
IMS Manual XX = Serial number assigned to the manual
Level 2 Document IMSP XX
IMSP = IMS system procedure
IMS procedures XX = Serial number assigned to the procedure

Level 3 and 4 Documents

Sl.
Document title Numbering system
No
1 IMS objectives and targets IMS-O&T-Serial number

2 IMS Management programs IMS -MP- Serial number

3 Master list of documents IMS -ML-01

4 Master list of records IMS -ML-02

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Control of Documents

Level 3 and 4 Documents (continued)

Work Instruction (WI)

Checklist (CL) AA : BB - XX
Approved supplier list (ASL) AA = Originating Dept Code
Master list (ML) BB = Abbreviation of the document
Audit plan (AP) XX = Serial number assigned to it
Quality Plan (QP)

IMSF-XX-F-YY

IMSF = IMS Format

Formats
XX = Serial Number of the associated procedure
F = Format
YY = serial number assigned to a particular format

All documents shall indicate their current revision status and the revision date.

Numbering system for design documents are maintained by design department.

5.3 Preparation, approval, revision and re-approval of documents

Responsibility for Authority for

Preparation and Responsibility for approval and
Document description
incorporation of Review Re-approval (of
revisions revisions)

IMS Manual ISO coordinator /MR ED/MD MD

IMS procedures Functional Head MR MD

Level 3 & Level 4 Designated Concerned Concerned

Documents Employee Functional Head/MR functional Head

5.4 Control of document changes (Revisions)

5.4.1 IMS Manual (Level 1 document)

The Management representative shall identify the need for changes in the IMS manual
based on inputs such as audit findings, changes in the organization structure, change in

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Control of Documents

organization’s business, changes in work practices due to adoption of technical advances,

changes in responsibilities and authorities of personnel etc.,

Whenever revisions are made to IMS manual, such revisions shall be carried out in
accordance with document control procedure described in the section 0.4 of IMS Manual.

5.4.2 IMS Procedures (Level 2 documents)

The originating function’s head shall determine the need for revisions based on inputs such
as, audit findings, suggestions received for improvement, changes in work practices due to
adoption of technical advances, changes in responsibilities and authorities of personnel etc.,
The functional head shall incorporate changes in the procedure and it shall be reviewed by
the top management and approved by the MD.

Whenever IMS system procedures are revised, brief note of revisions shall be provided at
the end of the document.

5.4.3 Level 3 and Level 4 documents

The originating functional head or his designated employee shall determine the need for
revisions based on inputs such as, audit findings, suggestions received for improvement,
changes in work practices due to adoption of technical advances, etc. The designated
employee shall incorporate changes in the document and it shall be reviewed and re-
approved by the functional head.

Whenever Level 3 documents are revised, functional head shall ensure that

a) Copy of the revised document is given to MR in order to update the master list of
documents.
b) Previous revision document is identified as “OBSOLETE”,
c) Old issues are retrieved Form all users and disposed off suitably,
d) Documents of pertinent revision only are made available with the users.

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Control of Documents

Functional Head’s designated employee shall retain the documents of previous revision for
reference purpose. Whenever a document is revised, whole document shall be issued under
next revision number.

6.0 Issue and control of documents

6.1 General
MR shall maintain Master list of IMS documents to indicate the latest revision status. For this
purpose, he shall coordinate with all functional heads and obtain information on revision
status of level 3 and level 4 documents.

Personnel responsible for issue and control of documents shall maintain Document issue
register in order to ensure timely issue of documents to all concerned.

Issuer and user, both are responsible for ensuring availability of pertinent issue of
documents at all points of use.

6.2 Issue and control of IMS Manual and IMS Procedures (Level 1 and 2)

MR shall maintain the Master copy (Original) of IMS Manual and all IMS procedures. These
documents shall be identified as MASTER COPY on the rear side of the documents.

MR shall issue and control these documents by posting them in the company website
http://www.ksphc.in. The user may take print-out of these documents and it shall be the sole
responsibility of the user to ascertain and maintain and use the latest document as posted in
the referred website.
Superseded document shall be identified with OBSOLETE COPY seal. Obsolete documents
shall be disposed-off after minimum retention period as per IMSP 02 – procedure for control
of records.
6.3 Issue and control of Level 3 documents

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Control of Documents

Designated employee of concerned functional head shall maintain the Master copy (Original)
of level 3 documents. These documents shall be identified as MASTER COPY on the rear
side of the documents.

Designated employee of concerned functional head shall issue and control these documents
through “Document issue register”. Documents issued under this methodology shall bear the
seal CONTROLLED COPY on front face of document at an appropriate place.

6.4 Issue and control of Level 4 documents

Generally printed Forms are used for recording purposes. A copy of this (Blank copy) is
treated as a document. A blank copy of these formats are uploaded onto company website.
The user of these forms can download the required forms and use them as necessary.
Originator of records (A Form in which data are filled) may issue the records to the relevant
functions for identified purposes.

7.0 Control of documents and data of external origin

7.1 Standards related to IMS management system

MR shall be responsible for control and updating of applicable National / International

Standards pertaining to IMS Management Systems. Updating of standards can be done
either by subscribing with the originating agency or their authorized distributors or, by
periodically verifying the status in respective website of the originating organizations. Master
list of documents shall include this to reflect the latest revision status of these documents.

7.2 Standards related to product and processes (construction related)

Design Dept. shall be responsible for control and updating of applicable National /
International Standards related to construction materials and their testing, construction
processes. Updating of standards can be done either by subscribing with the originating
agency or their authorized distributors or, by periodically verifying the status in respective
website of the originating organizations.

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Control of Documents

7.3 Standards related to product design

Design Dept. shall be responsible for control and updating of applicable National /
International Standards and reference books related to product design. Updating of
standards can be done either by subscribing with the originating agency or their authorized
distributors or, by periodically verifying the status in respective website of the originating
organizations.

Note: Documents provided by the client organization is treated as customer property

and are handled in accordance with the requirements of ISO 9001:2008 Clause
number 7.5.4

8.0 Control of documents in electronic media

Originator of documents shall ensure that necessary checks and controls have been
established to approve, incorporate change and re-approve by provisioning of password
protection for the specific fields.
System Administrator to ensure the access control to these documents by giving password
protection with write protection. Subsequently access to change/revise the document shall
be controlled through password protection.

Originator shall ensure that back up of data is taken on any update made to preserve and
protect the data.

9.0 Records

Sl. Authorizing Custodian of Retention

Name of the Record
No Personnel record Time

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Control of Documents

Designated Designated Till the issue

Issue details of Level 3 and employee of employee of of next
1
4 documents concerned concerned revised
functional head functional head documents

10.0 Reference

a) ISO 9001: 2008 Clause Number 4.2.3

b) ISO 14001:2004 Clause Number 4.4.5
c) IMS Manual section / Clause 3.2.3

11.0 Associated Documents

a) Procedure for control of records IMSP 02

Approved by : Managing Director

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