: 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