360° Regulatory Assistance We advise on regulatory requirements connected to a wide variety of issues, such as the commercialization of pharmaceutical products and medical devices, conduct of clinical trials, promotional activities for pharmaceutical products and medical devices, as well as any relating data protection issues. We assist clients in the drafting and execution of compliance programs and organizational models relating to corporate liability pursuant to Legislative Decree no. 231 of 2001, also by acting as external members of their Compliance Committees.
Contracts and Corporate We are especially skilled in drafting and negotiating licensing and partnering agreements, research and development agreements, joint ventures arrangements, clinical trials agreements, co-promotion and co-marketing agreements. We know the rules applicable to agreements with health care professionals and institutions and the pitfalls to avoid. We also advise life science clients in corporate transactions such as acquisitions, mergers, investment and financing agreements, joint ventures and shareholders agreements, as well as any relating service (due diligence investigations, drafting of corporate resolutions, etc.).