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