We provide assistance in drafting and reviewing clinical trial and pharmacovigilance agreements. We take account of the Client’s role and responsibilities (sponsor, investigator, CRO or healthcare facility) and of the nature of the study. Depending on the Client’s needs, we work on individual agreements or on the entire set of contracts for the project. We handle the definition of the parties’ roles and responsibilities, the identification of the timelines and obligations of each party involved, the rules governing the processing of personal and health data and the transparency obligations, as well as the coordination with sector-specific legislation and with the authorisations required. Our approach is to deliver clear, balanced and compliant agreements that protect the Client from a legal and data protection standpoint and ensure that the trial and the pharmacovigilance activities are carried out properly.