Over 250 highly skilled consultants and analysts partner with clients to achieve their strategic goals by leveraging Clarivate expertise and data. Our tailored insights and real world data drive innovation to improve patient lives and create a healthier tomorrow. Throughout the Biopharma and MedTech product lifecycle, Clarivate provides end-to-end solutions and helps answer specific questions from bioinformatics to market access, to pharmacovigilance and beyond. We advance the development and rollout of novel products that have a material impact on our customers’ performance. We believe human ingenuity can transform the world and improve our future.
Our Life Sciences and Healthcare consultants provide strategic guidance, professional services, custom data and technology enablement to over 80% of the world’s top 50 pharmaceutical companies. Meet some of our experts
We help companies advance their drug discovery, preclinical proof-of-concept, and regulatory activities. Clarivate’s translational science expertise, skilled teams of regulatory and commercial experts and assets such as the Centre for Medicine Research (CMR) combine to offer a highly reputable source of pharmaceutical industry metrics and insights. By providing perspective, data and insights across the development spectrum, we complement client teams in generating long term value.
Our deep domain expertise and data-driven analysis provides customized, actionable solutions for our clients in the areas of new product planning, portfolio strategy, pricing, and market access. Leveraging Clarivate proprietary data, real world evidence and deep consulting expertise we can help you make faster, more informed strategic decisions on your toughest challenges and most significant opportunities.
We provide integrated health economics and outcomes research, value communications, and real world evidence strategy to the life science industry, partnering with client teams over the lifecycle of a brand. Our team consists of technical experts including health economists, statisticians, medical writers, in-house graphic designers, commercial assessment analysts, systematic reviewers, and COA specialists, enabling us to provide bespoke, end-to-end solutions across the product lifecycle.
We offer highly customized, use-case-specific data deliveries including bespoke databases, data files, and workflow solutions built to exact specifications. Innovative solutions such as ClaRITA (Clarivate Regulatory Intelligence Tracker, a companion of Cortellis Regulatory Intelligence) provide decision support to key business leaders leveraging internal and external data assets. Our team of experts and their proven methodologies create unique tools that allow clients to make data-driven decisions with speed and certainty across the drug/device development lifecycle.
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