This episode of the podcast is tailored for pharmaceutical companies planning to organize meetings, conferences, or scientific events, both in Italy and abroad.We’ll delve into the key regulations and compliance requirements that must be met, with a particular focus on events related to the promotion of medicinal products manufactured or marketed by the same company.In Italy, the law establishes specific procedures to ensure transparency and integrity, preventing conflicts of interest and safeguarding the quality of disseminated information. Among these is the obligation to obtain prior authorization from the Italian Medicines Agency (AIFA), which must be requested at least 60 days before the event begins, as outlined in Article 124 of Legislative Decree 219/06.If your company is planning a scientific event, this episode will guide you through the requirements and steps necessary to ensure regulatory compliance. 

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