Internal Audit Schedule Template - ISO 9001

ISO 9001:2015 - QMS.9.2.1 - QR - Internal Audit Schedule

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 Schedule? Why do I need it in my Quality Management System (QMS)?

• This template provides a structure for planning when internal audits will take place in the organisation, and identify the areas of the system that will be audited, it will identify the auditor performing the audit and allow the organisation to plan to ensure that all areas of the system that require auditing are covered and that the audits take place on time.

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.