White Papers

Executive Summary Signal detection is a critical component of modern pharmacovigilance. As the volume of safety data grows and global regulations tighten, traditional tools and manual methods often fail to keep pace. Companies need smarter, faster, and more compliant solutions...

Executive Summary Pharmacovigilance Agreements (PVAs) and Safety Data Exchange Agreements (SDEAs) are foundational to regulatory compliance in drug safety partnerships. Yet, organizations continue to rely on manual methods that are inefficient, prone to errors, and leave them vulnerable to missed...

Executive Summary Pharmacovigilance (PV) teams today are burdened by outdated systems, high costs, and regulatory complexity. Traditional safety databases often struggle to keep up with increasing workloads and global compliance demands. Clinevo Safety Database offers a next-generation alternative: a cloud-based,...

Executive Summary Literature monitoring is a crucial component of pharmacovigilance (PV), ensuring safety data is captured from published scientific sources. However, traditional approaches are time-consuming, expensive, and prone to errors. Clinevo Literature Management introduces an AI-powered, cost-effective, and regulatory-compliant alternative...

Executive Summary Case intake is the critical first step in pharmacovigilance (PV), but traditional methods remain inefficient, error-prone, and fragmented. Manual processes and lack of intelligent automation result in increased compliance risks, delays, and duplicated efforts. Clinevo Case Intake revolutionizes...