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Domande reali. Risposte affidabili.
Risposte chiare, puntuali e affidabili su regolamenti, compliance e trasparenza nel settore sanitario.
Navigare il nuovo scenario normativo del Sunshine Act italiano? Un supporto competente fa la differenza.
Per questo abbiamo riunito un team di professionisti con una profonda esperienza nella rendicontazione Sanità Trasparente—pronti ad accompagnarti nel percorso verso una conformità sicura e consapevole.
Come funziona:
- Esplora i profili degli esperti e le loro aree di specializzazione
- Invia la tua domanda tramite il modulo
- Il nostro team analizzerà la richiesta e risponderà direttamente oppure pubblicherà la risposta nella nostra sezione FAQ in continuo aggiornamento
Roberto Cursano
Partner
Delfino e Associati Willkie Farr & Gallagher LLP Studio Legale
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A former official of the Italian Ministry of Health, Roberto has significant experience in the healthcare and life sciences industry.
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
Delfino e Associati Willkie Farr & Gallagher LLP Studio Legale
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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.
Mauro Teresi
Counsel
Simmons & Simmons
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With over a decade of experience in product liability and regulatory matters related to a wide range of medicinal products and medical devices, Mauro supports clients in domestic and cross-border commercial litigation and arbitration, early case assessment, and alternative dispute resolution procedures.
A member of the European Pharmaceutical Law Association (EPLA), Mauro also has broad expertise in healthcare and life sciences contracts and regulatory compliance across the entire product lifecycle—spanning clinical trials and investigations, market access, pricing and reimbursement, post-market surveillance, transparency, promotion, and advertising.
He regularly advises companies across sectors—including life sciences, IT, automotive, chemicals, consumer goods, and electronics—on product safety requirements, product recall management, regulatory risk, and internal investigation processes.
Mauro is recognized by The Legal500 for his work in Healthcare & Life Sciences, with clients describing him as: “Mauro Teresi brings deep knowledge and experience to matters, trustable and dependable.”
Edoardo Lazzarini
Former Senior Ethics & Compliance Officer, Southern Europe (Italy, Spain, Portugal)
Haleon | TAKEDA
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Edoardo, formerly a MedTech compliance officer, brings over 25 years of expertise in compliance and transparency. A recognized thought leader, Edoardo has led ethics programs across top pharmaceutical companies and offers strategic insights into Italian compliance practices.
Recent Engagements
- Community Event – Milan – February 26th, 2025
- Actively running Discovery Programs with 20 pharmaceutical companies, 10 medical device companies, 3 labs, and 1 cosmetics company.
- Transparency Reporting Workshop – Milan – December 17, 2024
- Hands-on Workshop: From Spend to Telematic Register – Milan – November 12, 2024
- Italian Sunshine Report: Hands-on Workshop by Experts – Milan – October 14, 2024
Upcoming Events
Ned Mumtaz
PFIZER | OTSUKA
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Ned is a global expert in transparency reporting with extensive experience producing high-quality, compliant reports for over 150 international pharmaceutical companies. He has held leadership positions at Pfizer and Otsuka and is renowned for his work in delivering precise and reliable reports.
Recent Engagements
- Community Event – Milan – February 26th, 2025
- Transparency Reporting Workshop – Milan – December 17, 2024
- Hands-on Workshop: From Spend to Telematic Register – Milan – November 12, 2024
- Italian Sunshine Report: Hands-on Workshop by Experts – Milan – October 14, 2024
Upcoming Events
Marialaura Boni
Counsel
Osborne Clarke
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