Italy's health agency unveils new decree for device registration

02/2/2010 | Clinica (subscription required)

Effective Feb. 6, all device makers with new products on the market are required to comply with the Italian health ministry's updated regulations for the registration of medical devices. The new decree also reduces the amount of data that must be supplied by companies when re-registering products in several categories including class I devices and active implantables.

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