The CE Mark and European Union (EU) Directives are a form of product certification. Organizations that manufacture machinery, medical devices, medicinal products, food, pressure vessels, toys, personal protective equipment, electronic devices, animal feeds, and veterinary products and who intend to sell or are currently selling to the EU may be required to comply with specific product standards. Compliance with these standards is mandatory. Organizations that fail to meet these requirements risk having their products pulled from the EU market and fines.
Organizations should determine through research which directive(s) apply to their product(s). Some directives require the existence of a formal quality system (e.g. ISO 9001). If a formal quality is required, Internal and Lead Auditor training should be conducted.
CE Mark Fast Track!
Which Organizations Should Be Involved?
Organizations who manufacture and sell (or intend to sell) the products listed above to the EU.
All pricing is stated in US dollars and is only for services provided in North America. International Pricing is available upon request. Course prices are per course and do not include course materials.
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