JOrdan
REGULATORY AUTHORITY: The Ministry of Health (MOH) oversees medical device regulation through the Jordanian Food and Drug Administration (JFDA).

CLASSIFICATION SYSTEM: Jordan accepts both the EU and FDA classification models.

TIMEFRAME: The approval process takes between four and eight months, depending on whether lab testing is required.

LICENSE VALIDITY: Licenses issued in Jordan expire when the device’s previously obtained license (from the USA, EU, or Japan) expires.

AUTHORIZED REPRESENTATIVE: A local authorized representative is required.

Last updated on March 17 2015.



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For​ more information on registration in Jordan, check out the following articles on our blog:
Country at a Glance: Jordan
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