Life Sciences and Healthcare Consulting Services
Improving patient lives by helping clients discover, develop and bring new treatments and devices to market
Our passion is to partner with clients to achieve their strategic goals in delivering safe, effective and commercially successful treatments to patients faster. Throughout the Biopharma and MedTech product lifecycle, Clarivate consultants provide end-to-end solutions and transformative intelligence, using industry-leading products like Cortellis and Real World Data.
Our teams fuel innovation in Research and Development, Commercial Consulting Services and Technology and are right by your side as you improve patient lives and create a healthier tomorrow.
Our consulting services
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. We also 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. 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 offer highly customized, use-case-specific data deliveries including bespoke databases, data files, and workflow solutions built to exact specifications. Innovative solutions such as the 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.
Our consultants provide and interpret best in class medical claims, offering a deeper view into US and international patient care and reimbursement information across inpatient and outpatient settings. We combine robust methodologies, deep therapy area and data science expertise with longitudinal and connected life sciences-grade real world data to accelerate your strategy. Services include aiding in data utilization, guiding through disease-specific nuances, or overseeing integrations. We are adaptable and well-organized to meet clients’ requirements – from delivering standardized dashboards to integrating and mastering our RWD with Clarivate formulary, affiliations or provider mapping data, so you can act with confidence.
A pharma story from the heart of Europe
How Gedeon Richter partnered with Clarivate consultants to transform regulatory workflow
Our latest thought leadership
AI and clinical diagnostics: following the road less travelled
The artificial intelligence (AI) revolution has created a remarkable opportunity to transform medical diagnostics by significantly enhancing the accuracy, speed, and efficiency of diagnosing patients. AI algorithms analyze medical images,…
The role of artificial intelligence or machine learning in conducting systematic literature reviews now and in future
AI and systematic literature reviews: potential benefits and use cases Good quality evidence is the hallmark of any successful roadmap to access. Systematic literature reviews (SLRs) and meta-analysis are generally…
