CE markingindicates that a product has been assessed by the manufacturer and deemed to meet EU safety, health and environmental protection requirements. It is required for products manufactured anywhere in the world that are then marketed in the EU

ISO 9001:2015specifies requirements for a quality management system when an organization:needs to demonstrate its ability to consistently provide products and services that meet customer and applicable statutory and regulatory requirements, and.

ISO 14001:2015specifies the requirements for an environmental management system that an organization can use to enhance its environmental performance.

ISO 13485:2016specifies requirements for a quality management system where an organization needs to demonstrate its ability to provide medical devices and related services that consistently meet customer and applicable regulatory requirements.

The Supplier Ethical Data Exchange (Sedex) isa not-for-profit, membership organisation that leads work with buyers and suppliers to deliver improvements in responsible and ethical business practices in global supply chains

The SA8000 Standard and Certification System provide a framework for organizations of all types, in any industry, and in any country to conduct business in a way that is fair and decent for workers and to demonstrate their adherence to the highest social standards.

A Capability Maturity Model Integration (CMMI) isa training program for professionals to learn process improvement and how to guide an organization through a process to project completion. The CMMI Institute offers this course with additional training to prepare you for certification