Accelerate clinical trial timelines and easily navigate the global regulatory landscape.

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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.

 

Optimize clinical performance and regulatory workflows with industry-leading intelligence.

Clinical consulting services

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:

  • Customized clinical dashboards
  • Indication-specific landscapes
  • Clinical investigator/ key opinion leader (KOL) selection
  • Trial protocol design

Regulatory consulting services

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:

  • Interactive dashboards
  • Regulatory newsletter spotlights
  • Regulatory requirements by country
  • Trend landscaping
  • Pharmacovigilance monitoring
  • Post-market surveillance
  • Custom data curation and analytics

Strategy development

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.

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"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..."

Eloise Hennebique

Regulatory Professional,
Bayer Corporation

Benefit from a unique combination of expertise and data science.

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.

Trusted experts who specialize in pharma R&D data science.

100 +

Analysts and consultants

9 K+

Drug programs

1.5 K

Drugs launched

2 K+

Drugs under development

Partner with us.

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.

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Stay on top of industry trends with BioWorld.

Receive daily insights on the latest biopharma news and medical technology advances to better inform crucial R&D decisions at the earliest research stages.

Learn more

Highlights of BioWorld’s coverage of ASCO 2019

Japan approval world-first for tumor-agnostic Rozlytrek

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See how we can deliver customized solutions that address your specific needs.

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