FDA-CE CERTIFICATIONS

FDA - CE ISO Product Import and Export Certifications

An export certificate is a type of official assurance, providing an importing country with confirmation from the government that your product or commodity meets certain standards and requirements.Not all countries or all products require them.
If required, the export certificate accompanies a consignment to its destination country, confirming the consignment's compliance with specific standards and requirements. An approved export certificate is provided to the appropriate border agency of the destination country – in either electronic or paper form – to help clear your product into that country. Certification is almost exclusively done for products exported for commercial purposes. However, certain countries require an export certificate for product destined for personal consumption, for example, fish caught while sport fishing.

What are FDA Export Certificates?

Firms exporting products from the United States are often asked by foreign customers or foreign governments to supply a "certificate" for products regulated by the Food and Drug Administration (FDA). A certificate is a document prepared by FDA containing information about a product's regulatory or marketing status.

What does CE certified mean?

CE marking is an administrative marking that indicates conformity with health, safety, and environmental protection standards for products sold within the European Economic Area (EEA). ... The CE marking is the manufacturer's declaration that the product meets EU standards for health, safety, and environmental protection.

The ISO 9000 family of quality management systems is a set of standards that helps organizations ensure they meet customers and other stakeholder needs within statutory and regulatory requirements related to a product or service.