Mark Hammar
March 13, 2018
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Automate your ISMS implementation and maintenance with the Risk Register, Statement of Applicability, and wizards for all required documents.
Documentation to comply with ISO 27001 (cybersecurity), ISO 22301 (business continuity), GDPR (privacy), and NIS 2 (critical infrastructure cybersecurity).
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Documentation to comply with ISO 27001 (cybersecurity), ISO 9001 (quality), ISO 14001 (environmental), ISO 45001 (health & safety), NIS 2 (critical infrastructure cybersecurity) and GDPR (privacy).
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Documentation to comply with MDR and ISO 13485 (medical device), ISO 27001 (cybersecurity), ISO 9001 (quality), ISO 14001 (environmental), ISO 45001 (health & safety), NIS 2 (critical infrastructure cybersecurity) and GDPR (privacy).
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Documentation to comply with AS9100 (aerospace), ISO 9001 (quality), ISO 14001 (environmental), and ISO 45001 (health & safety), and NIS 2 (critical infrastructure cybersecurity).
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Documentation to comply with IATF 16949 (automotive), ISO 9001 (quality), ISO 14001 (environmental), and ISO 45001 (health & safety), and NIS 2 (critical infrastructure cybersecurity).
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Get instant answers to any questions related to ISO 9001 (QMS) and ISO 14001 (EMS) using Advisera’s proprietary AI-powered knowledge base.
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With the new release of ISO 45001, the internationally recognized standard that replaces OHSAS 18001, we now have a greater assurance of what the requirements for documented information will be. In the new Occupational Health & Safety Management System (OH&SMS), this requirements section is one of the common elements that you will see handled the same way in all of the ISO management system standards, including ISO 9001, ISO 14001, ISO 27001, and many others.
Here is what this change could mean to your OH&SMS.
In the current revision of OHSAS 18001, which is the current standard for an OH&SMS, there are separate requirements for documents and records within the standard. Documents are controlled under clause 4.4.5, which requires rules for approval, review & update, changes, legibility, and relevancy of available documents for use in the processes. Records, on the other hand, are controlled by clause 4.5.4, which requires rules for records to be identifiable, properly stored, protected, retrievable, and disposed at the end of a specified retention period. If you currently have an OH&SMS in place and you are using the requirements of OHSAS 18001, then these are the rules that you will already have in place for your documents and records.
In the ISO 45001 standard, there is now a new term that replaced “documents and records.” These materials are now called “documented information.” This concept includes all documented procedures and records that are currently mentioned in OHSAS 18001. Throughout the standard, where OHSAS 18001 would say you need a documented procedure or record for a certain requirement, ISO 45001 states that you need to retain documented information for certain requirements. Also, within ISO 45001 clause 7.5 (Documented information), there are requirements that need to be in place for all documented information. These include creating, updating, and control of documented information. The required steps include:
For more on OH&S documentation, see these articles: How to structure health & safety documentation according to OHSAS 18001, and Which criteria to apply when deciding about OHSAS 18001 documentation.
The requirements for what needs to be documented essentially remain unchanged. This means that you still need certain documented information to meet the standard, as well as other documented information that you decide is necessary for your management system. Looking at the actual requirements for what you need to do with documented information, the requirements are basically the same as the ones that have been there for documents and records. These requirements, in a nutshell, are:
So, have the requirements changed that much? The answer is no. In general, if you have a method to control your documented procedures and a process to control your records, there is really nothing to change as the requirements for control are really the same. In fact, many companies already had one procedure for control of both documents and records, and this is also acceptable with the new standard requirements.
There is also nothing in ISO 45001 that says you need to start using the term “documented information” in your company. If other terminology works for you, then keep using it; the certification auditors will need to follow the terms you use, and this would not be the first time. So, take a minute to go over your procedure, or procedures, and see that everything is covered (it probably is). If this works for you, there is no need to confuse your employees by changing it, but keep in mind that the term “documented information” now includes more than just the procedures and records that were encompassed before. If, however, you think that you could benefit from changing the way you do things, then this is a good time to make that change. You will likely be going through other updates and training as you implement ISO 45001 after it is released, so this improvement can be communicated easily.
As always, it is important to remember why you are implementing an OH&SMS in the first place. It is not to please the ISO, or even to satisfy the auditors; you have this management system to better control and improve your OH&SMS. Make sure that the processes you implement work for you to achieve this improvement goal, rather than just being there to satisfy the requirements of the standard. You want your OH&SMS to give you benefits, not to be a burden.
To find out more about what is currently required for documentation in ISO 45001, see this white paper: Checklist of Mandatory Documentation Required by ISO 45001.
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