MedBoard

MedBoard is designed for regulatory affairs, clinical research, market intelligence, and post-market surveillance (PMS) teams in medical technology, pharmaceuticals, and life sciences. It brings together specialized information and work tools for researching requirements, tracking product and market developments, and organizing evidence and compliance work. Users can search regulatory, clinical, market, and safety information, including regulations, guidance, clinical literature and trials, product records, approvals, recalls, safety alerts, and adverse events. Regulatory tools support intelligence monitoring, compliance workflows, and management of product registrations. Clinical research tools support systematic literature reviews, including screening and reporting, alongside reference and citation management. Market and PMS features help teams monitor products and manufacturers, maintain watchlists, and review vigilance information. Analytics, product profiles, and task management help organize findings and team work. The platform also includes an AI research assistant for questions and summaries across regulatory, clinical, market, and PMS topics. MedBoard is suited to organizations that need a shared workspace for research, regulatory intelligence, clinical evidence, and product safety monitoring; available tools depend on the modules used.

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