International News

Regulatory “Changes” to Device Registration in Italy

By Evangeline Loh and Sage Farrar, Emergo Group | March 15, 2010

As Evangeline and I prepared this brief, a story from my freshman year of college continued to come to mind. I had just arrived on campus for the first of seven days called “Orientation Week.” We were given an agenda, tightly packed with activities, icebreakers, introductions to college life, various lectures, meet-and-greets with the deans, a memorable talent show and brunches galore.

The activities were scheduled from early morning until late at night, and my professed new best friends and I, all of us self-admittedly overachieving, thought it was a requirement to attend all of the events. So there we were, day six, unaccompanied by the vast majority of our incoming class who had opted out of most events. The last event was scheduled the day before classes would commence, and it was a day of selfless service—hard, manual labor to give back to the community. In theory it sounded wonderful, but it was a Sunday, we were exhausted, and it was pouring outside. In a moment of regrettable weakness, we decided that we would not go.

That Sunday, while I guiltily slept in, I heard a knock at my door. It was my residential adviser politely informing me that I had neglected to read the fine print of the agenda. “Volunteer” day actually was required. I remember laughing then, as I am now, at the notion of “mandatory volunteerism,” the irony and comedy of which never ceases to amuse me.


Italian Registration Update

Since our last column, changes to the registration requirements for medical devices in Italy have been issued, namely that registration no longer is required for Class I devices for which European authorized representation is established outside of Italy. But, alas, as is the case with most happy and too-good-to-be-true tidings in the regulatory world, there is often a slight catch.

As you may be aware, Italy’s Decreto 20 Febbraio 2007 (Decree of Feb. 20, 2007) required manufacturers or their designated entities to register their medical devices (except IVDs, which need to be notified through a different process) with the Italian Ministry of Health Database, if the medical devices are to be sold in Italy. The complete listing of all registered devices is organized into a database. The last Euro News column detailed that the deadline for the re-registration of devices introduced to Italy prior to May 1, 2007, was postponed once again until March 31 this year. This delay had been to give the Italian Ministry of Health additional time to simplify the database and modify the current expectations of the National Directory.

Just recently, new legislation was introduced. Decreto 21 Dicembre 2009 (Decree of Dec. 21, 2009) went into effect on Feb. 6, and supersedes the directive issued in February 2007. The major change is that Class I medical device registrations with the Italian Ministry of Health (MoH) are no longer required for manufacturers whose European authorized representative is located outside of Italy. Note that registrations are still required for Class I devices of manufacturers whose European authorized representative is located in Italy and, of course, Italian manufacturers of Class I medical devices.

The Italian National Health Service, Servizio Sanitario Nazionale, or SSN, is the healthcare system in Italy. The SSN encompasses multiple health-related agencies, as well as all public health authorities, facilities and hospitals. Therefore, its reach is unending. The catch to the seemingly eased and “lessened” requirements is that only devices that are registered are available to the vast SSN. In fact, the listing of all of the devices available to the SSN is termed the “Repertorio,” and it is important to note that all products registered with the Repertorio are subject to a fee of 100 euros. Thus, although Class I devices whose manufacturers have European representation outside of Italy are exempt from registration requirements, if they wish to market their devices within the SSN, they still must register their devices. Unfortunately, however, specifics were not detailed in the decree. In fact, the issue of SSN registration was only briefly mentioned as an option for manufactures of Class I devices to participate in “voluntary registration,” but, again, the specifications of which were not explained.

In addition to the section on “voluntary registration,” the decree of Dec. 20, 2009, made it a goal to lessen some of the requirements for registration of Class IIa, IIb, and III medical devices, as well as active implantable medical devices. Similar to the vagueness on the registration process for the SSN, the degree to which these requirements have been assuaged for higher-risk class medical devices and implantable medical devices is not clear. In fact, there are several parts of the new decree that are uncharacteristically elusive; so much so, that the Italian Ministry of Health scheduled an internal meeting in mid-February to discuss the issues. Essentially, the decree omits crucial details, and while the official minutes and summary of the internal MoH meeting have yet to been made public, it is anticipated that the ministry will issue guidance to mitigate the confusion that the decree has presented.

What we now understand, and perhaps was not clear in the text of the decree, is that the “voluntary registration” pertains to the need for Class I devices to be registered in order to be marketed within the SSN system.

Furthermore, it is likely that these devices that are “voluntarily” registered also will be subject to the 100 euro Repertorio fee, although this too is not outlined in the decree. So, in practice, unless manufacturers wish to sell their products only to private medical facilities and not to the larger (and more lucrative) SSN, the new decree does little to enact registration reform. This, of course, gave rise to the story of my day of mandatory volunteerism (which, for the record, I completed, rain and all).

Reviewing Requirements

If you are a manufacturer with European authorized representation outside Italy:

• Class I registrations are not required, unless the manufacturer would like to make their Class I devices available within the SSN, in which case device registration (and Repertorio fee) is required.

• Registrations are required for Class IIa, IIb, and III medical devices.

• If your products were introduced prior to May 1, 2007, you must go through the steps of re-registering with the Italian Ministry of Health no later than March 31, 2010.

If you are a manufacturer with European authorized representation in Italy:

• Registration is required for all medical devices.

• Those devices that were marketed prior to May 1, 2007, must be registered by March 31, 2010.

We hope this has helped to highlight some of the changes to the regulatory landscape in Europe, and more specifically, to explain the “double-edged sword” of the new lightened registration requirements in Italy that for the majority of manufacturers (foreign and domestic), do little to lessen regulatory requirements.

As more information becomes available, and in the event that the Italian Ministry of Health issues guidance on the topic, this column certainly will keep you informed. In the meantime, for anyone planning volunteer activities, as a word of advice, mandatory volunteerism (in our opinion) really goes against the spirit of giving and empowerment.


Evangeline Loh, Ph.D., R.A.C., is vice president of regulatory affairs for Emergo Group, an international consulting firm providing regulatory, quality assurance and distribution consulting services. Emergo has offices in the United States, Europe, Japan, China, Canada, Mexico and Australia. Evangeline can be reached at evangeline@emergogroup. com. Sage Farrar is a regulatory research associate at the Emergo Group.

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