Clinical and Regulatory Services

Predict and expedite your clinical trial timelines and navigate the regulatory environment.

Pharmaceutical and medical device companies are faced with a range of challenges in clinical development, clinical operations, competitive positioning and regulatory.

As the single largest area of spend for drug and medical device development, implementing a cost effective clinical strategy is an imperative:

  • Maintaining a competitive view on scientific intelligence and clinical strategy
  • Incorporating increasing complexity into clinical trial design while managing costs
  • Considering how personalized medicine and rare disease targets further increase clinical trials costs
  • Utilizing benchmarking performance data to optimize clinical trials execution
  • Understanding the regulatory risks and costs associated with new/emerging markets
  • Keeping track of regulatory changes and updates
  • Comprehending the implications of regulatory changes and communicating these to the organization

The Clarivate Analytics professional services team provides a range of services to optimize your clinical performance and to provide clear and concise regulatory intelligence to assist you in navigating today’s complex regulatory environment.

Teresa Fishburne

Teresa Fishburne

Director, Clinical and Regulatory Professional Services

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