10 Improvement [ISO 45001]

What is Improvement for ISO 45001?

Your organization should actively seek out and realize improvement opportunities that will better enable it to achieve the intended outcomes of its OH&S management system.

10.1 General

Potential sources of improvement opportunities include the results of analysis and evaluation of health and safety performance, compliance, internal audits and management reviews.

Workplace inspection for improvement

Improvement often does not take place on a ‘continual’ basis. Sometimes improvement can be affected reactively through corrective actions, incrementally overtime, by a step change or breakthrough, creatively through innovation or by re-organization and transformation.

Look out for objective evidence that improvement is taking place. However, while improvement does not need to be continuous, it does need to be evidenced as occurring.

Related Information You Might Find Useful

Next ISO 45001 Clause

Each ISO 45001 Clause Explained

Updated: 30th April 2022
Author: Richard Keen

Richard Keen

Richard Keen

Richard is our Compliance Director, responsible for content & product development.
But most importantly he is ISO's biggest fanboy and a true evangelist of the standards.
Learn more about Richard

ISO Checklist

Don’t Try to Manage It All Alone!

Our ISO Auditors and Quality Manager Trainers have been in this industry for years, and since 2002 we’ve been providing thousands of small businesses and large corporations with the tools they need to get certified.

Instead of trying to create everything you need to follow this process from scratch, use ours. We have procedures, templates, checklists, process maps, forms and gap analysis tools to help you control your documented information without missing a single input or output.

Before you invest all the hours reinventing the wheel, before you spend countless dollars outsourcing the task — try our templates.


  QMS
ISO 9001
EMS
ISO 14001
OH&S
ISO 45001

Nonconformity & Corrective Action Procedure

The purpose of this procedure is to establish the process for identifying, documenting and analyzing non-conformities and mitigating their impacts by implementing appropriate corrective actions. Your organization’s quality management system is geared toward the proactive elimination of actual and potential deficiencies.

Non-conformities in products, services, processes and our management system are investigated and action implemented to prevent their occurrence.

Forms & Reports also included:

  • Control of Nonconformity & Corrective Action Process Activity Map
  • Non-conformance Report
  • Non-conformance Log
  • Concession Request
  • Concession Request Log
  • Corrective Action Report
  • Corrective Action Log
  • Nonconformity & Corrective Action Process Map

>> Free Download - Control of Calibrated Equipment Procedure - this will give you a good idea of what to expect when you purchase the procedure.

>> I'm looking for more Procedures

$19 USD

add to cart

$19 USD

add to cart

$19 USD

add to cart

  • Supplied as fully-editable MS Word or Excel files
  • All the templates use styles – making reformatting and rebranding a breeze
  • Immediate download

Pay by Credit Card, Debit Card, PayPal or Apple Pay.
Credit card, PayPal or ApplePay

money back guarantee


We are 100% confident in the quality and contents of our products. Used by thousands of organizations around the world, our templates have been sold online since 2002.

Please read our Money Back Guarantee.

Are The Templates Suitable For You?

Bought by Small Businesses and Large Corporations our templates have been sold online and CD since 2002.

Used by:

  • Small Businesses – dentists, accountants, engineers
  • Large organizations – hospitals, power plants, aircraft manufacturers

The Templates are used by first timers following our step-by-step, clause-by-clause guidance documents; and experienced Quality Managers wishing to streamline and improve their existing documentation.

The application of our templates is scalable and generic; regardless of the size and type of organization. The elements that form the quality management system are the same.

Five Reasons To Choose Our Templates

1. Our customizable templates save you time and money by offering a streamlined process to create your quality documentation

2. They’ve got everything you need in one simple template

3. Proven to work our templates have helped thousands of businesses big and small achieve certification

4. Documents use styles to make reformatting and rebranding a breeze

5. Our templates are generalizable for any industry or sector. The application of our templates is scalable and generic; regardless of the size and type of organization.

FAQs About Our Templates

Ask Us a Question

More Information

 

ISO 9001 Client images