Professional Documents
Culture Documents
REVISION HISTORY
REFERENCE DOCUMENTS
Documents referenced in this procedure are applicable to the extent specified herein.
1. Purpose
To have a distinctive serial number for each document so that each document can
be uniquely identified as to its type, issue number and the relevant clause of ISO
9001:2000.
To ensure that
• Quality System Documents (QSDs) are approved for adequacy before use
• QSDs are reviewed and updated as necessary and documents so updated
are re-approved
• changes and current revision status of documents are identified
• relevant versions of applicable documents are available at points of use
• documents remain legible and readily identifiable
• obsolete documents are identified and their unintended use is prevented
• documents of external origin are identified and their distribution controlled
2. Scope
This procedure covers all documents of the quality management system. This
document lays down the procedure for initiation of work for preparing new quality
system documents, for amending and revising existing documents and the
authority for taking such actions and for reviewing, approving and issuing them.
It also lays down control procedure to ensure that all amendments and only latest
version of the documents are in use. It also lays down steps for retrieval of
superseded documents from points of use and their destruction or for retaining
copies for archival purposes.
3. Applicability
This procedure is applicable to all Quality System documents prepared by any one
in or for RIL except quality records.
4. Definitions/Abbreviations
5 MR Management Representative
6 CC Controlled copy
7 CL Check List
11 WI Work Instruction
5. Responsibilities
Approval: Managing Director
Issue: Management Representative (MR)
Implementation: Management Representative (MR)
6. Procedure
REFERENCE
Step ACTION
ACTIVITY DOCUMENT
No BY
NUMBER
6.1 Quality Manual (QM) MR RILQMV1.0
Quality Manual (QM) is codified as RILQMV1.0
where RIL is RAMKY INFRASTRUCTURE LIMITED,
QM is Quality Manual and V1.0 is the Version
Number. Whenever Issue Number changes Version
Number is also increased.
6.2 Quality System Procedures are codified as MR -
RIL/SYS/PRO/NN, where ‘RIL’ denotes the
Organization; ‘SYS’ denotes SYSTEM; ‘PRO’
indicates Procedure; ‘NN’ denotes procedure
number for given function/ process.
REFERENCE
Step ACTION
ACTIVITY DOCUMENT
No BY
NUMBER
Each System or Departmental Operating Procedure MR -
carries a Revision History in the front page of the
document. A tabular column of Reference
Documents is in the second page and this is
followed by (1) Purpose, (2) Scope, (3)
Applicability, (4) Definitions / Abbreviation, (5)
Responsibilities, (6) Procedure detailing the
activity, Action authority and reference documents,
(7) Process measure (8) Quality Records and (9)
Forms Used.
6.3 Annexure are codified as AN-a/XX/Y where AN MR -
represents Annexure and ‘a’ indicates Annexure
number. XX indicates type of manual and Y
indicates section reference of the manual.
REFERENCE
Step ACTION
ACTIVITY DOCUMENT
No BY
NUMBER
Quality System Procedures are prepared by MR/MD
Manager (QMS), reviewed by MR and approved by -
MD. Departmental Operating Procedures and work
instructions are prepared by department personnel
concerned, reviewed by Head of Department and HOD/MD
approved by MD.
6.9 Re-Approval -
REFERENCE
Step ACTION
ACTIVITY DOCUMENT
No BY
NUMBER
6.13 The Original Quality System Documents are MR
maintained by the MR in a file called “Current
Quality System Documents”.
REFERENCE
Step ACTION
ACTIVITY DOCUMENT
No BY
NUMBER
6.19 The master list is updated whenever an MR RIL/SYS/FOR/02
amendment or revision for a QSD is issued
6.20 Obsolete Documents
Invalid and / or obsolete documents are collected MR -
back from all copy holders and from all points of
issue and use.
6.21 Obsolete documents when retained for purposes of File
knowledge / back reference / legal requirements MR/ MD
are stamped "OBSOLETE" on each page in blue
and filed in a file named "Obsolete documents".
The Managing Director is the authority to authorize
retention of such obsolete documents.
6.22 Documents of External Origin -
7. Process Measures
8. Quality Records
1 Document Distribution Soft & Lock & Key ISO Wing 2 years
Register Hardcopies
2 Master List of Documents Soft & Lock & Key ISO Wing 2 years
Hardcopies
3 Document Change Soft & Lock & Key ISO Wing 2 years
Requests Hardcopies
4 New Document Requests Soft & Lock & Key ISO Wing 2 years
Hardcopies
5 Document Transmittals Soft & Lock & Key ISO Wing 2 years
Hardcopies
Disposal: by shredding
Disposition Authority: Managing Director
9. Form(s)
Forms required for this document: