ISO 9001 & ISO 45001 Audit Checklist XLS

Utilize this Integrated Management System Audit Checklist Template to assess your progress toward ISO 14001:2015 EMS implementation. It contains 29 Excel worksheets that correspond with one or more clauses/subclauses from ISO 14001 (such as Leadership).

Each ‘shall” requirement is assumed to meet, until an “x” is entered in Columns F-H for further review and scoring of audit requirements. This provides for more accurate scoring of audit requirements.

Identifying Key Performance Indicators (KPIs)
When selecting KPIs for your business, make sure they directly align with its goals and intended results. They must also be quantifiable so you can measure progress made toward meeting those goals, while at the same time focus on critical success factors – activities which, when executed successfully, lead to enhanced performance for your company.

Consideration should be given to how your KPIs impact other departments, in order to ensure they do not overlap or distract from one another. Furthermore, take note of measuring both lagging and leading indicators.

Once you have selected KPIs, they must be implemented into your QMS by documenting how they will be measured, monitored and reported upon. This should include your measurement methodology and frequency of reporting as your auditor will require this documentation to review them.

Identifying Key Processes
Our fully editable internal audit checklists include the certifiable requirements from each of the management system standards as questions to help evaluate your management systems. They provide the documented information required by individual Standards as well as allow you to compare performance over time or across divisions.

Are there processes in place to identify, investigate and address incidents, nonconformities and opportunities for improvement? Are these processes effective?

Have you clearly and rationally defined the scope of your quality management system, along with documented proof that this has been implemented?

Are you able to demonstrate how your relationships with external providers impact on your ability to consistently meet customer, statutory and regulatory requirements? Have procedures in place that ensure any nonconforming products or services provided by external suppliers are recalled, segregated, quarantined, returned for correction or re-provision in a timely fashion? Additionally, do you record, analyze and act upon results of external supplier self-evaluations assessments?

Identifying Key Personnel
Conducting internal audits to comply with ISO compliance requirements can be time consuming, complex, and stressful. By using an internal audit checklist template you can streamline this process and make it more manageable.

This checklist features 29 worksheets that each cover one or more clauses from ISO 14001:2015 standard and are designed to assist organizations with tracking progress towards full EMS implementation.

It also covers occupational health and safety management practices to assist organizations in providing their employees with a safe working environment while adhering to OHS regulations.

Top management must regularly evaluate its OH&SMS in order to ensure it remains effective in meeting needs, legal, and other requirements – this is a key requirement of the standard. Audit results must be documented and retained as evidence of its effectiveness; often these documents serve as support documents when self-declaring conformance or registration – more commonly referred to as certification.

Identifying Key Documents
Legally executing documents requires going through a verification process that ensures their signers are who they claim they are. That’s why signNow, with its digital certificate for signers’ identity verification and two-factor authentication features, is such an ideal online signing solution.

Successful ISO 9001 certification audits depend heavily on the quality of your documentation. Your auditors will expect to see information that supports all processes within your QA management system – for example your quality manual, procedures, work instructions, and forms – and must demonstrate that any non-conformances have been addressed and quality has improved as part of this evidence.