Pharmaceutical and medical device companies face a range of challenges across clinical development, clinical operations, competitive positioning and regulatory submission. As the single largest area of spend for drug and medical device development, implementing a cost-effective clinical strategy is imperative to speed up your clinical trial timelines, track milestones and easily navigate the regulatory environment.
Our Clinical and Regulatory Consulting teams optimize your clinical performance and deliver the clear and concise regulatory intelligence you need to navigate today’s complex regulatory environment. Work with us to maximize your portfolio’s return on investment by accelerating innovation in disease understanding, R&D decision-making and drug and device assets.
Transform and accelerate your clinical trials with experts who have problem-solving skills that deliver results. Our experienced consulting team can advise you on the critical decisions relating to clinical development, clinical operational strategy and competitive positioning.
Key services include:
Navigate regulations around the world with insights and guidance from our regulatory consulting team. We apply our knowledge and expertise to your data to help you make the best decisions.
Regulatory services include:
Leverage data to provide comprehensive analysis for strategy planning.
To maintain a competitive view on scientific intelligence and clinical strategy, it’s important to develop and implement a cost-effective clinical strategy. Leveraging data from our proprietary databases, our team provides comprehensive analysis that informs your clinical strategy.
"Thanks to [Clarivate] I have the right information to plan my worldwide submissions faster, in compliance with the various local requirements. [Clarivate] is also a very powerful tool to set up regulatory submission strategies efficiently..."
No one else provides the breadth of data you need – from biomarkers, targets, biological pathways, omics, gene variants to pipelines, clinical trials, competitive information and regulatory guidelines.
Unrivaled data science expertise, evidence-based consulting and independent advice across the pharmaceutical R&D value chain.
Benefit from proprietary data-mining and surveillance pipelines, analysis algorithms, data integration and visualization tools.
Analysts and consultants
Drugs under development
Our accredited global alliance program delivers value-added solutions by combining offerings from Clarivate with other technology and service providers. Partner with us to drive profitable growth, increase revenue and deliver greater value to your customers.
Receive daily insights on the latest biopharma news and medical technology advances to better inform crucial R&D decisions at the earliest research stages.