Continual Improvement Tracker - ISO 9001

ISO 9001:2015 - QMS.10.3 - QR - Continual Improvement 

Our Medical Device Quality Assurance and Regulatory Affairs document templates have been created by fully qualified and experienced professionals at Patient Guard, a Quality Assurance and Regulatory Affairs Service provider. The templates have been specially written to ensure that they meet the basic requirements needed for each clause/section of the standard or regulation the templates relate to. We have carefully curated the templates to ensure they are easy to follow and adapt to make them specifically modified to your business needs. All the templates are fully editable Microsoft word documents allowing you to have complete control over the templates which can then be modified to suit your company branding/marketing requirements.

Why do I need to include a Continual Improvement Tracker in my Quality Management System?

• The ISO 9001 standard requires that your organization shall continually improve the suitability, adequacy and effectiveness of the quality
  management system.
• This helps a an organisation to track what improvements have been made to the quality management system 
  
• By operating a continual improvement programme the company can be more effective in understanding what works and does not work in terms of improvement initiatives. 
  

How will the Complaints Procedure help my organisation?

• The purpose of this template is to help your organisation to track any improvements that have been made in order to improve the quality management system.
• This enables the company to specifically identify when an improvement was made and what the outcome of the improvement was. This allows the company to make better informed decisions based on what worked well and what didn't work so well when implementing past improvements to the QMS. 

If you would like further information on our wide range of templates or have any suggestions for improvements that require support in addition to our templates in the form of other Medical Device Quality Assurance or Regulatory Affairs services, contact us at qmsregs@patientguard.com.