15 luglio 2025 | online 10:00 AM – 10:45 AM CET

Gli obblighi derivanti dal Sunshine Act. Come prepararsi?

Le maggiori criticita’ di natura legale ed operativo-tecnologica.

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Le sessioni si terranno in italiano.

Esclusivamente per i professionisti del settore Life Sciences – Partecipazione gratuita

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Unisciti ai nostri esperti legali e operativi per un aggiornamento su come affrontare nel concreto i principali obblighi previsti dalla legge.

Durante la sessione parleremo di:

Cosa significa essere “pronti” dal punto di vista legale e digitale
Come impostare correttamente responsabilità, tempistiche e strumenti interni
Come affrontare le criticità più comuni
Come evitare errori nelle fasi preparatorie e nella rendicontazione

Una sessione pensata per chi sta già analizzando la normativa e vuole passare agli aspetti operativi.

Esclusivamente per i professionisti del settore Life Sciences – Partecipazione gratuita

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Profili dei Relatori

Roberto Cursano

Partner
Studio Legale Delfino e Associati Willkie Farr & Gallagher LLP

He focuses on regulatory matters, including research and development, manufacturing, marketing of medical products, product recalls, interactions with healthcare professionals and organizations and related transparency obligations and litigation before the Supreme Court and the Council of State. Additionally, he assists with the setting-up of compliance models aimed at
preventing corruption-related crimes corporate liability.

Roberto participates in training and tutoring in the master’s degree program on clinical trials of pharmaceutical products at the University of Rome Sapienza. He also regularly publishes articles and scientific contributions. He frequently hosts and participates in seminars and presentations on pharmaceutical and administrative law matters.

Riccardo Ovidi

Counsel
Studio Legale Delfino e Associati Willkie Farr & Gallagher LLP

Riccardo has substantial experience advising companies operating in the healthcare and life sciences sector on regulatory matters throughout the entire lifecycle of their products, from research, development and manufacturing to marketing and promotion, distribution, post-market surveillance, product recalls, interactions with healthcare professionals and organizations and related transparency obligations.

Additionally, he assists with the formation of compliance models aimed at preventing corporate liability.

Riccardo also has broad experience in assisting domestic and foreign companies in navigating the export control and sanctions landscape by advising them in connection with the export and import of controlled items and business transactions with sanctioned countries, preparing license applications, carrying out audits and delivering trade compliance trainings.

Riccardo is a regular speaker in seminars on healthcare, compliance and export control matters as well as the author and co-author of various articles and publications on international and local journals.