Audit your Environmental Management System for compliance with ISO 14001:2015. Check your EMS meets ISO standards.

Use this comprehensive supplier corrective action report form to accurately investigate on the root cause of the nonconformity, including the direct cause, detection cause, and systemic cause. This supplier corrective action report form also contains a permanent corrective actions and recurrence prevention section, where quality managers can detail unlimited corrective actions, identify expected completion date, and provide objective evidence after completion.

Use this template when doing a visual check of the entire property.

This weekly manufacturing quality control checklist helps maintain standards across your operation. 1-10-100 Rule: This rule states that detecting quality problems early in the manufacturing process is less costly than catching a quality challenge later in the manufacturing process: https://www.workclout.com/post/1-10-100-rule-cost-of-quality

This PPE checklist template is used to ensure workers safe by going through a proper protective equipment list

An 8D report template is used to document a comprehensive root-cause analysis based on the 8 Disciplines of Problem-Solving, previously known as the Team-Oriented Problem-Solving. 8D teams can easily generate a detailed report with the use of this template.

Quickly gather the facts. Collect evidence about an incident, accident or injury. Conduct full investigations quickly with this incident report template.

An FMEA template aims to identify potential problems in a process, product or design and prevent their adverse effects on customers. Monitor the implementation and effectiveness of corrective actions with the use of this template. Enable your team to easily describe the process function, identify the mechanism of failure and determine the RPN. Create and complete corrective actions and validate the FMEA with digital signatures.

The Pressure Equipment Directive (PED) (2014/68/EU) applies to the design, manufacture and conformity assessment of stationary pressure equipment with a maximum allowable pressure greater than 0,5 bar. The directive entered into force on 20 July 2016. The Pressure Equipment Directive aims to guarantee free movement of the products in its scope while ensuring a high level of safety. The implementation of the Directive is supported by a set of PED Guidelines and guidance documents: Guidelines - pressure equipment directive 97/23/EC (related to the former PED) Guidelines - pressure equipment directive 2014/68/EU These guidelines are not legally binding – instead, they help to ensure that the directive is applied consistently. Unless otherwise indicated, they represent the unanimous opinion of the Working Group Pressure composed of representatives of the national authorities of the Member States.

Use this digitized checklist to let customers specify details for maintenance work. A work order is a paper or electronic document that outlines a service request or maintenance activity that must be performed. Using a work order template saves time and helps to ensure that information collected is consistent and complete.

A CAPA Report form is designed to help identify, address, and prevent the occurence of regulatory and organizational non-conformance. This can be used by compliance officers when formulating a corrective action to resolve the issue, and a preventive action to lower the risk of its recurrence.

Use this root-cause analysis template to analyze a recurring problem and help eliminate the root causes. Begin by describing the issue and its impact. Next, list potential reasons why the issue happened and identify the root cause and take/attach photo evidence for verification. Provide a prevention strategy and recommend solutions before completing the RCA template with digital signatures.