1. DOCUMENTATION REQUIREMENTS Based on ISO 9001:2008

2. The quality management system documentation shall include the following.
Documented statements of a quality policy and quality objective.
The quality policy ensures clear focus of quality across the organization and direct employee activities on quality, customer focus and continual improvement.
The quality objective ensures that customer requirements are met and also continually improve the performance of the organization through the quality management system. They will be set and they will be reviewed in management review meetings.
A quality manual.
The quality manual shows the scope of quality management system; incorporating details of justification for any exclusion (it shows functional organization structure)
Documented procedures and records required by the international standards.
Documents including records, determined by the organization to be necessary to ensure the effective planning, operation and control of its processes.(quality manuals & quality procedures)

3. The extent of quality management system documentation can differ/change from one organization to another due to the following factors-
The size of organization and type of activities
The complexity of processes and their interactions.
The competence /ability of personnel/workers.
The quality manual
The organization shall establish and maintain a quality manual that includes,
The scope of the quality management system, including details of and justification/explanation for any exclusion /leaving out.
The documented procedures established for quality management system, or reference to them.
A Description of interaction between the processes of the quality management system.

4. Control of document
Documents required by the quality management system shall be controlled, and documented procedures shall be established to define the controls needed.
To approve documents for adequacy prior to issue
To review and update as necessary and re-approve documents
To ensure that changes and the current revision status of documents are identified
To ensure that relevant versions of applicable documents are available at points of use.
To ensure that documents remain legible and readily identifiable.
To ensure that documents of external origin determined by the organization to be necessary for the planning and operation of the quality management system are identified and their distribution controlled.
To prevent the unintended use of obsolete documents and to apply suitable identifiable to them if they are retained for any purpose.

5. Controls of records
Records established to provide evidence of conformity to requirements and of effective operation of the quality management system shall be controlled.
The organization shall establish a documented procedure to define the controls needed for the identification, storage, protection, retrieval, retention, and disposition of records.
Storage of records,
Records shall be stored in either soft or hard copy.
Protection,
All records shall be protected against damage; soft copy shall be protected from heat, dust, water and magnetic field. Hard copy records shall be protected from heat, dust, water, and kept in a safe place.
Records shall remain legible, readily identifiable and retrievable.

6. EXTRA INFORMATION

7. Demonstrating conformity with QMS Standard & Objective Evidence
It may be able to demonstrate conformity without the need for extensive documentation.
The organization has to be able to provide objective evidence of the effectiveness of its processes and its quality management system. Clause of ISO 9000:2005 defines “objective evidence” as “data supporting the existence or variety of something” and notes that “objective evidence may be obtained through observation, measurement, test, or other means.”
Objective evidence does not necessarily depend on the existence of documented procedures, records or other documents, except where specifically mentioned in ISO 9001:2008. In some cases, (for example, in clause 7.1(d) Planning of product realization, and clause Monitoring and measurement of product), it is up to the organization to determine what records are necessary in order to provide this objective evidence.  
Where the organization has no specific internal procedure for a particular activity, and this is not required by the standard, (for example, clause 5.6 Management Review), it is acceptable for this activity to be conducted using as a basis the relevant clause of ISO 9001:2008. In these situations, both internal and external audits may use the text of ISO 9001:2008 for conformity assessment purposes.

8. Objectives of documentation:
a)   Communication of Information
as a tool for information transmission and communication. The type and extent of the documentation will depend on the nature of the organization’s products and processes, the degree of formality of communication systems and the level of communication skills within the organization, and the organizational culture.
b)   Evidence of conformity
provision of evidence that what was planned, has actually been done.
c)    Knowledge sharing
to disseminate and preserve the organization’s experiences. A typical example would be a technical specification, which can be used as a base for design and development of a new product.
 Documents may be in any form or type of medium, examples: paper, magnetic electronic or optical computer disc , photograph, master sample

9. DOCUMENTATION
the amount and detail of documentation required to be more relevant to the desired results of the organization’s process activities.
the minimum amount of documentation needed in order to demonstrate the effective planning, operation and control of its processes and the implementation and continual improvement of the effectiveness of its QMS.
It is stressed that ISO 9001 requires (and always has required) a “Documented quality management system”, and not a “system of documents”.
Any documentation approach that you adopt should always provide value-added for the management of your quality system, not simply meet the auditor’s/ registrar's requirements.

10. Terms and Definitions relating to Documents
Document - Information and its supporting medium
Procedure - Specified way to carry out an activity or a process  (Note: Procedures can be documented or not)
Quality Manual - Document specifying the quality management system of an organization
Quality Plan - Document specifying which procedures and associated resources shall be applied by whom and when to a specific project, product, process or contract
Record - Document stating results achieved or providing evidence of activities performed
Specification - Document stating requirements

11. QMS- DOCUMENTATION Documentation requirement Systematic and orderly
Written policies and procedures
Ensure common understanding
Shall include provision for:
Identification
Distribution
Collection
Update
Withdrawal
Archiving
Retention/retrieval

12. Documents required
The quality management system documentation shall include:
documented statements of a quality policy
and quality objectives;
a quality manual
documented procedures required by this International Standard
4.2.3 Control of documents
4.2.4 Control of records
8.2.2 Internal audit
8.3 Control of nonconforming product
8.5.2 Corrective action
8.5.3 Preventive action
documents needed by the organization to ensure the effective planning, operation and control of its processes, and
records required by this International Standard;
All the documents that form part of the QMS have to be controlled in accordance with clause of ISO 9001:2008, or, for the particular case of records, according to clause

13. Additional Documents to ADD VALUE
An organization could add value to its QMS and demonstrate conformity by the preparation of other documents, even though the standard does not specifically require them. Examples may include: - Process maps, process flow charts and/or process descriptions - Organization charts - Specifications - Work and/or test instructions - Documents containing internal communications - Production schedules - Approved supplier lists - Test and inspection plans - Quality plans
All such documents have to be controlled in accordance with the requirements of clause and/or 4.2.4, as applicable

14. Records Required by ISO 9001:2008
CLAUSE RECORD REQUIRED
5.6.1 Management reviews
6.2.2(e) Education, training, skills and experience
7.1(d) Evidence that the realization processes and resulting product fulfil requirements
7.2.2 Results of the review of requirements related to the product and actions arising from the review
7.3.2 Design and development inputs relating to product requirements
7.3.4 Results of design and development reviews and any necessary actions
7.3.5 Results of design and development verification and any necessary actions
7.3.6 Results of design and development validation and any necessary actions
7.3.7 Results of the review of design and development changes and any necessary actions
7.4.1 Results of supplier evaluations and any necessary actions arising from the evaluations
7.5.2(d) As required by the organization to demonstrate the validation of processes where the resulting output cannot be verified by subsequent monitoring or measurement
7.5.3 The unique identification of the product, where traceability is a requirement
7.5.4 Customer property that is lost, damaged or otherwise found to be unsuitable for use
7.6(a) Basis used for calibration or verification of measuring equipment where no international or national measurement standards exist
7.6 Validity of the previous measuring results when the measuring equipment is found not to conform to requirements
7.6 Results of calibration and verification of measuring equipment
8.2.2 Internal audit results and follow-up actions
8.2.4 Indication of the person(s) authorizing release of product.
8.3 Nature of the product nonconformities and any subsequent actions taken, including concessions obtained
8.5.2(e) Results of corrective action
8.5.3(d) Results of preventive action

15. QMS- DOCUMENTATION HIERARCHY
I Level
Policy
What do we do?
Why?
Policy Objectives
Stated once
II Level
Procedures
Who?
When?
Where?
Calibration
QA Procedures
Audit Processes
III Level
Work Instructions or Practices, Technical Data
How?
Work Instructions,
Inspection Instructions, Standard Operating Practices, Drawings, Specifications, Standards
IV Level
Records or Proof
Evidence-;all the records and forms which are generated by the working system. 1 2 3 4

16. RBS - Quality Management Systems
Requirements for service quality by public service organisations.

17. DOCUMENTATION REQUIREMENTS
General
The organization shall document the following:
Service quality manual;
Citizens’ charter;
Any other document needed by the organization for effective planning, operation and control of its service and service delivery processes; and
Records required by this standard (see 4.4).

18. Service Quality Manual
The organization shall establish and maintain a service quality manual which includes:
Scope of service quality management system;
Service quality policy;
Service quality objectives;
Complaints handling objectives;
Responsibility and authority of personnel at relevant levels within the scope of this standard;
Documented procedures required by this standard;
Other documents, needed by the organization for effective planning, operation and control of its service and service delivery processes, or reference to them; and
Description of service processes including service delivery processes at the customer interface and those needed to directly support them (see 7.2).

19. Control of Documents
All the documents required by this standard shall be
approved for adequacy prior to issue;
reviewed periodically, updated as necessary and re-approved. The changes made shall be identified; and
legible and identifiable indicating their current revision status.
The organization shall
maintain a master list of all documents related to the scope of this standard which also identifies their current revision status;
maintain distribution list of all such documents;
ensure that the current versions of applicable documents are available at points of use;
ensure that obsolete documents, if retained for any purpose, are suitably identified to prevent their unintended use; and
ensure that the documents of external origin are identified and their distribution controlled.
A documented procedure shall be established to define the controls needed for the above.

20. Control of Records:
Records (including files) shall be established and maintained to provide evidence of conformity to requirements and for the effective operation of the management system for service quality.
The records shall remain
legible,
readily identifiable and
easily retrievable.
The method of
identification,
storage,
protection,
disposition of each record,
their retention time and
responsibility
for each of these activities shall be established in a documented procedure.

21. SULFO RWANDA INDUSTRIES
PREPARED BY
Note: All the above companies are ISO certified
BRALIRWA
NAKUMATT RWANDA
SULFO RWANDA INDUSTRIES

22. THANK YOU !