Document Managment
Document Managment
Purpose
This procedure states the structure of company standards system documents. To ensure that the document is updated,
controlled and distributed to proper location throughout “COMPANY NAME”.
Scope
This document is used for controlling internal documents and external documents that is related with the Quality,
Environment, Safety and other concern management system documents, data, and records; This procedure defines the
guidelines for coding system used in formulating document number for each Standard, Procedure, Check sheets, Work
Instructions Memo, and other related documents generated by the entire processes / sections in the plant.
Locations / Distribution
Environment, Health & Safety Maintenance & Equipment Services Quality Assurance & Technology
Material Judgment Room Raw Material Warehouse
Finished Good Warehouse
Production Planning & Control Tyre Testing Room
Human Resource & Administration
Purchasing
Division A (Mixing, Extrusion, Calendering & Material)
Division B (Tyre Building, Curing & Finishing)
Reference
- Record
Form1 (DP-Q-01) Document Master List
Form2 (DP-Q-01) Document Distribution List
Form3 (DP-Q-01) Request for Additional Copy of Document
Form4 (DP-Q-01) Issued/ Revised Control Document Approval
Form5 (DP-Q-01) External Origin Documents Master List
Form6 (DP-Q-01) Revision History Record
PROCEDURE DP-Q-01 Revision 02
Effective Date : DD/MM/YYYY
Document Management Page 2of 12
Table of Content
Purpose…………..………………………………………………..……………..……. 1
Scope ……………………………………………………………..……………..……. 1
Definition………………………………..………………...……………………..…… 1
Locations/Distribution...……………………………………………………………… 1
Reference...………………………………………………………………………….
1
Table of Contents……………………………………………………….…..…………. 2
1. General ………………….………………………………………………..………… 3
2. Document Structure……………………………………………………..…………. 3
3. Writing Guideline……………………………………………………….…………. 4
4. Document Validity………………………………………………………………….. 5
8. Document Reviewed………………………………………………………………... 9
1. General
Documents and data contain information approved for present and future use in our system, on a repetitive and
long-standing basis. Documents supplied to us by external source and used in the system are also included examples
of document as company rules, procedures, Standards, Schedules, Standard Operation Procedure, Working
Instruction, and external documents such as inspection procedures, test procedures and equipment manuals,
technical standards, manufacturing specifications, standard machine settings, and external standards such as product
standards, testing standards and regulations documents.
2. Document Structure
The company standards system documents are categorized into Company rules, Standards, and procedures. Company
rules include on all documentation on all management elements, Definitions are given below:
Rules include document on all management elements (Quality Policy, Quality Objectives etc).
Standards is a rule or principal that is used as a basis for judgment. It is an established guiding principle,
administrative law, regulatory or statutory requirement created to provide a criterion reference for common
judgment or decision in a given condition or situation.
Examples: Management systems standard (QMS), Yokohama Standards, Customer requirements, Industry
Standards, Statutory & Regulatory requirements
Procedures a fixed step by step sequence of activities, or series of actions (with definite start and end point)
that must be followed in the same order to correctly perform a task. It describes the activities of each
functional unit.
Standard Operation Procedure is a set of fixed instructions or steps for carr”Company Name”g out routine
operations or procedure prescribed for repetitive use in a given operation or in a given situation, in accordance
with agreed upon specifications aimed at obtaining a desire outcome and supports the mechanics of procedures
and standards.
Working Instruction sheet is a description of the specific tasks and activities that are temporary in nature
and/ or yet to be standardized within Plant.
External Documents issued by the various functional organizations are recorded as internal and external
official correspondences.
Figure 1
3. Writing Guideline
3.1 The following are the writing guideline for company rules, procedure, standard (general rules), operation
procedure (general rules) and working instruction exclude the form (record sheet).
i. The document structure and format shall be
The body text font Times New Roman, Size: 10.5, Paragraph: 1.5 line spacing, Justified.
ii. The first page of each document shall contain the following items.
Purpose: To explain the purpose, why issue the document
Scope: Where, What the document covers or exclude
Definition: What the meaning of abbreviation word is.
Locations/Distribution: Where the documents issued and stored.
Reference: Indicates the reference documents or related documents, In case of do not have the reference
document, no indicated will be permission.
If the above said contents are not to be covered in one page, it may be extended to page Two.
Flow Chart: At the end of each document, to summarize the activities of that document (If necessary)
iii. The next page shall contain the table of contents.
PROCEDURE DP-Q-01 Revision 02
Effective Date : DD/MM/YYYY
Document Management Page 5of 12
iv. Succeeding pages after table of contents page shall be the main detail of document.
3.2 For standard and operation procedure (below the general rules or its equivalent), document format and structure
is decided by the document originator.
3.3 For the form or record sheet the document format is decided by the document originator.
v. Revision History: At the last page of finished procedure with or without flow chart. The revision history will
indicate the issuance date, revision No., Reason for revise, Issued by (originator), reviewer and approval person.
4. Document Validity
A Company standard system document contains the name, position and original signature of the approval authority
and issue date. Issued date is considered as effectively date. The approval authority on any documents and changes
in the company standards and systems are as following
Note: * For some situations, the approval / reviewer authority might not be available, then the document shall be
approved by the higher authority in that command line.
by each section. A log sheet should be maintain for the same in soft copy. See below for the sample
5.4
SOP: Standard Operating Procedure DW-△-
Second digit: W is the symbol for SOP
WI: Work Instruction WI-△-YY (WI for Work Instruction)
MR (Material Review) Sheets : Dp-MR-YY (Dp: Plant Code)
Business Trip Report: Dp-BTR-YY (Dp: Plant Code)
Symbol Means Code Definition
△ Issuance Process - ** Same as the above (Standard)
YY Year code - Current year (last two digit);
sequential number - ** Same as the above (Standard)
5.5 Form (Record Sheet): Form R△ ()
Symbol Means Code Definition
Form The check sheet, attached - The attached document or the
Document format that use for the recording.
- The sequential No. will be started
sequential number
from 1,2,3 …
R△ Revision No. of Form - The revision No. of form (0, 1, 2,
3…)
Refer Code referring to Company Rule,
Refer the DR, DP, DS or DW
5.1,5.2, 5.3 Procedure, Standard or Working
number
and 5.4 Procedure No.
EX. Form 1 R0 (DP-Q-01)
PROCEDURE DP-Q-01 Revision 02
Effective Date : DD/MM/YYYY
Document Management Page 8of 12
6.1 Issuing of New Document or Revision. Any employee can initiate a document revision or a document need due
to changes in the internal system of the plant. The section head concerned, in turn, informs the document originator
or Document Controller (if no document originator is yet identified) what revisions need to be made to the
document. The originator shall be ensure that the document remain legible and readily identifiable. Identification
on changes made on the contents of the documents include used of underlining as long as purpose to identify
revision is clear.
6.2 Preliminary Planning. The document originator assesses the document to be written or revised. This assessments
includes the purpose for the document, and points of Improvements for the Quality Management System.
6.3 Document Code Assignment. After the document originator wrote or revised his document, consults Document
Controller (QA & Tech. Section) about the document code that will use.
6.4 Review and Approval. The final document is reviewed and approved by the assigned document reviewer and
approver.
6.5 Registering Approval. The document originator prepares the set of approval documents, and issues the Form 4
(DP-Q-01). The document originator submits all of them to Document Controller 3 days before effective date (that
indicated on the column “Issued Date”). Document Controller is responsible for registering (updating the master
list) in the “Document Master List: Form 1 (DP-Q-01)”, stamping “ORIGINAL DOCUMENT” on the behind
page of all-original controlled document, maintain and distribution.
6.6 Distribution. Document Controller is responsible for distributing the controlled copies to concerned Process
Owner with locations after having duly marked on the font of all approved copies with “CONTROLLED COPY”,
recording the location where distributed on “Document Distribution List : Form 2 (DP-Q-01)” and collected the
obsolete documents prior to issuance of revised ones.
PROCEDURE DP-Q-01 Revision 02
Effective Date : DD/MM/YYYY
Document Management Page 9of 12
Note: No Tampering Allowed for any type of Documents e.g.: No writing on the documents or Photocopy
Document Controller is responsible for collecting and disposing all obsolete controlled copy documents due to
document revision. The obsolete original documents in the one level before current revision are stamping
“OBSOLETE DOCUMENT” and maintaining, the former revision shall be disposed.
Quality documents receiving (using) section or group should be responsible for handling of received documents
(receiving control, storage control) and for treatment of the documents after their usage (when documents became
obsolete).
If documents are received and stored through the electronic media, storage management shall be defined in quality
documents/ records storage procedure of the using Section or Group.
6.7 Request for additional copies. The person who requires an additional Controlled copy of a document shall
issued Form 3 (DP-Q-01) and get the approval from QA & Tech. Section or higher rank.
Document Controller stamped with a Controlled Copy and registered in the Document Distribution List for the
permanent used. All additional copies issued for temporary usage such as classroom instructions, reference & short
orientation must be return to Document Controller to prevent unintended use and shall be identify by
UNCONTROLLED COPY (such as for training purpose or references for external party) – used to
identify authorize of documents to persons requesting for official copy. Uncontrolled copies of documents
are not subject to retrieval but should be recorded on document control records.
8. Periodic Review
At least once a year, the document originator reviews each document and data for obsolescence and determines
whether revision of the document is necessary. Records of review shall be indicated on the document history sheet
of that particular document.
The person who is responsible to control the external document is indicated as the following
The External Origin Document distribution should be controlled by each responsible person, Form 5 (DP-Q-01)
should be used or the proper form is available, Ex. Yokohama Standard (YS) can be stored, Form 5 can be stored in
soft copy by the control in Server.
Document No.
DP-Q-01~
DP-Q-20
Document Name
Issuance Section
END OF DOCUMENT