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03 October 2022

Life Sciences

Stefano Giberti and Erica Benigni contributors for Chambers Medical Devices & Consumer Health Products 2022 Global Practice Guide

An overview of Italian regulations on medical devices, drugs and other products such as biocides and cosmetics, with particular reference to new technologies.

What rules apply in Italy on the cultivation and use of cannabis for medicinal purposes? Which services can be provided through telemedicine? How can a wearable be classfied as medical device?  What is a borderline product?

And also. The life cycle of a pharmaceutical product: from design to production, from marketing to communication. The Regulators Engagement and Enforcement and product liability. Last but not least, what is changing in the policy and legislative reform. A short but exhaustive guide.

Our Stefano Giberti and Erica Benigni describe the complex Italian regulation system in the prestigious Chambers Medical Devices & Consumer Health Products 2022 Global Practice Guide.

The Italian chapter available in the attached file. The entire guide available at the following link: Global Practice Guide

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