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European Commission Makes Final Decision On Cranberry Products

 
• By Amanda Maxwell

Several manufacturers in the EU have marketed cranberry capsules as medical devices to gain regulatory and marketing advantages. Others have lobbied against this "unfair practice." France took the matter to the European Commission, which took action – the first time the commission employed its "borderline"-product designation authority.

The European Commission's Regulatory Committee on Medical Devices has ruled that cranberry products cannot be regulated as medical devices. This is an important ruling for industry because it is the first time that the European Commission has used its "borderline" product decision-making authority.

In making its ruling, the committee voted in favor of an earlier draft commission decision. The decision was made in response to a request from French authorities. (Also see "

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