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15 June 2021

Life Sciences

The Life Sciences Law Review awarded Francesco Setti for his contribution to the 9th edition.

In the article written by Francesco are addressed and described the main requirements for a regulated drug during its entire life cycle .

In the chapter dedicated to Italy, Francesco describes the requirements that a regulated product must meet throughout its life-cycle, from discovery to clinical trials, the marketing authorisation process and post-approval controls. 

The article begins with a detailed description of the contents of the Pharmaceutical Regulatory , and then goes on to examine the procedures relating to pricing and reimbursement, administrative and judicial remedies, financial relations with prescribers and payers, special liability systems, and competition issues.


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