AS/NZS ISO 45001 Document Control Procedure

AS/NZS ISO 45001 Document Control Procedure

This document control procedure can assist your business to comply with AS/NZS ISO 45001 2018, Occupational Health and Safety Management Systems clause 7.5. Documented Information.

The procedure can help you to ensure that documented information is up-to-date, accurate, reliable, reviewed and formally approved.

$45.50 - Includes 10% Tax
Description

What is a Document Control Procedure?

A document control procedure outlines the process and methods for the administration, development and maintenance of documents. This is a requirement for compliance with AS/NZS ISO 45001 occupational health and safety management systems.

The Document Control Process

                              The Document Control Process

The objective of a document control procedure is to ensure that all relevant ‘documented information’ and its associated organizational knowledge is reviewed and approved by authorized personnel before issue.

Typical documents that are controlled by a document control procedure can include, but are not limited to:

  • AS/NZS ISO 45001 management manuals, procedures and related forms.
  • Formalised ‘documented information’ that is required.
  • Operational procedures, reports, forms and corrective actions.
  • Management review documents and mandatory documented minutes.
  • Specifications, designs and drawings, etc.
  • Formal electronic communications.
  • Documents addressing risks and opportunities and continual improvement records.
  • Documents related to interested parties and OH&S risks to compliance with international standards.

What is Document Control and Record Management?

Document control is the administration process and systematic control of documented information. The objective of document control is to ensure that documents are kept up to date, controlled, easily retrievable and released with the relevant approvals. Following a document control procedure ensures that only the most current version of a document is being used and that all users have access to the latest version.

Record management specifies the requirements for the identification, storage, security, recovery and retention time of records. The process can apply to all records that are defined within a company’s document register, or other record management system.

It is important that a company creates, captures and maintains full and accurate records of its activities, including outsourced, contracted or internet-based activities. Good record management plays a critical role in:

An effective OH&S management system process will ensure that:

  • All critical electronic OH&S documents will be maintained and backed up.
  • All hardcopy records that are created and updated will be protected from damage by storage in suitable compartments.
  • All necessary documents for proactively improving OH&S performance are retained. (e.g. records of consultation and participation of workers, injuries and illnesses, internal audits and all OH&S legal requirements).
  • An established documented quality assurance system is enabled.
  • Records subjected to regulated timeframes must be kept for the required period to enable an audit trail.
  • All archived records stored offsite will be maintained in a secure, suitable location.
  • Discarded records will be permanently destroyed/disposed of after retention periods have elapsed.

Note: Records should be situated for easy retrieval in case a backup is needed or a request for viewing by a nominated party.

Electronic Record Management

A company’s electronic records should be maintained within a record management system protocol and/or a recording database to prevent unauthorized access, destruction, alteration or removal and to provide easy access. A company’s network drives, storage media and related technologies and practices for maintaining electronic records must be designed, operated, regulated and maintained in such a way that records cannot be altered without the approval process before the document is published.

Availability, Traceability and Storage of Documents

The records of any reputable company should be legible, identifiable and traceable to the activity, product or service involved. Key document management system documentation should contain:

  • An issue date (and revision date where appropriate).
  • A standardized documented version control number.
  • The type of document.
  • The name of the approver of the document.

Note: No changes, amendments, inclusions or additions to current management system documentation, should be made valid unless authorized by management. Documents should always remain legible when document revisions occur.

Disposal of Documents and Records

Generally, there are two different methods of disposal for documents and records:

1. Restricted access or confidential – i.e. records that contain information about individuals, the information given in confidence, or records related to investigations. At the point of disposal, these sensitive records should be shredded.

2. Open access or normal records – these records can be destroyed using the usual methods of white paper recycling.

An organization’s management is responsible for ensuring that outdated or redundant documents are removed from all points of issue. Obsolete documentation requiring retention for legal, system evaluation or reference purposes should be identified and appropriately stored (archived) and managed.

Records should always be stored in areas that guarantee, as far as is reasonably practicable, protection against any disaster such as fire or flood.

Contents of this Document Control Procedure

  • Approval.
  • Purpose.
  • Scope.
  • Terms and Definitions.
  • Roles and Responsibilities.
  • Procedures.
  • Document and Record Management Process Overview.
  • Document and Record Management Process Flowchart.
  • Record Management (both paper and electronic).
  • Correspondence Protocol.
  • Letter Templates.
  • Emails.
  • Email Use.
  • Traceability, Storage and Availability.
  • Organizing Files by Date.
  • Electronic Records.
  • Document Control.
  • External Origin Documents.
  • Storage and Retention.
  • General Retention Period for Records.
  • Disposal Authority.
  • Information Technology.
  • Software.
  • Authorized Users.
  • Electronic Data Backup.
  • General Maintenance of Individual Computers.
  • Shut Down of Workstations by Users.
  • Electronic Virus Control.
  • Related Procedures, Forms and Documents.
  • Review Criteria.
  • Record Management.
  • References.

Why Choose to Buy this AS/NZS ISO 45001 Document Control Procedure

  • This 13-page AS/NZS ISO 45001 document control system procedure can provide you with a range of defined methods for the administration and maintenance of OH&S objectives, documents and records.
  • The procedure can help you ensure that documents are accurate, up to date, reviewed and approved by the relevant stakeholders and accessible to those who need them.

After purchasing this AS/NZS ISO 45001 document control procedure you will be able to:

  • Very easily edit and customize the template to create your own document control procedure.
  • Apply your own style, format and brand to the procedure.
  • Use it in any industry or sector regardless of the size or type of organization.

Availability and Use of this AS/NZS ISO 45001 Document Control Procedure

  • This AS/NZS ISO 45001 document control procedure is accessible to you right now by clicking the ‘Buy Now’ button.
  • The procedure will be delivered to you in fully editable Microsoft Word format for immediate and full use in your business.
  • There are no subscriptions, contracts or ongoing costs.

AS/NZS ISO 45001 Document Control Procedure Guarantee

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