Angelo Forte | Milan | Hogan Lovells

Angelo Forte

Associate Global Regulatory

Languages

Italian, English

forte-angelo

Angelo Forte
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  • Overview
  • Experience
  • Credentials
  • Insights and events

Angelo Forte is an associate of the Life Science & Healthcare Regulatory team in Italy. 

Angelo regularly assists local and international life sciences clients on a broad range of regulatory issues, such as the regulations on clinical trials and observational studies, including the drafting of related contracts, Good Clinical Practices, management of substantial amendments and adverse reactions, pricing and reimbursement procedures, early access tools and the use of technological tools in the life sciences industry.

Angelo also supports clients in complying with transparency obligations and anti-corruption regulations, as well as in the implementation of governance, internal control and compliance systems pursuant to Legislative Decree 231/2001.

Angelo graduated in 2020 from the Luiss Guido Carli University in Rome, where he also completed a Second Level Master’s Degree in 2024.

He is currently an LLM Candidate in Masters of Law at the King’s College in London. 

Representative experience

Assistance to several online retail platforms on product and advertisement requirements, marketing practices, and regulatory licensing requirements.

Assistance in negotiation and drafting of agreements with major Italian hospitals for the supply of an innovative gene-engineered therapy for rare diseases for a major pharmaceutical company.

Advice to various life sciences companies on compliance management, including donations, HCP/HCO interactions, anti-corruption, and transparency (Sunshine Act).

Advice to medical and tech firms on health apps, covering regulatory, privacy, and commercial aspects, including potential medical devices or PSPs classification.

Assistance to pharma companies in drafting and reviewing master services and clinical trial agreements, related standard operational procedures and routine advice on clinical trial regulations.

Assistance to several pharma companies in the alignment and integration of company clinical trial templates with the template prepared by the Italian Drug Agency.

Credentials

Education
  • Master of Laws (LL.M.), King's College London, 2025
  • Second Level Master’s Degree in Business & Company Law, LUISS Guido Carli University, cum laude, 2024
  • Laurea Magistrale in giurisprudenza (Master's Degree in Law), LUISS Guido Carli University, cum laude, 2020
Bar admissions and qualifications
  • Milan