Internal Audit Procedure - ISO 9001

ISO 9001:2015 - QMS.9.2 - QP - Internal Audit Procedure

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.

What is an Internal Audit Plan? Why do I need it in my Quality Management System (QMS)?

• Internal Audits are an integral process of ISO 9001, internal audits allow the organisation to monitor processes to ensure they are being carried out effectively in accordance with required procedures and work instructions, or highlights where a process or procedure needs to be updated to reflect best practice. 
• This internal audit procedure template covers all the requirements set out in ISO 9001 for the purposes of Internal Auditing ISO 9001 Quality Management Systems. 

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.