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Feasibility & Site Selection Solutions

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Select the right countries, sites, and investigators for your trial

Clinical trial feasibility and site selection analyses are a vital part of successful clinical trial planning. Leveraging the best data to determine your country-site-PI footprint is arguably the most important single factor when it comes to achieving enrollment within projected timelines and ultimately securing the results needed for evaluation against your endpoints.

At Citeline, we are proud to offer a solution that enables the full feasibility and site selection workflow from clinical trial landscapes, site and investigator experience and history, and knowledge of relevant patient populations for your protocol.

Discover how we put data at the heart of your decisions and support you in successfully delivering a trial that can run on time, on budget and without the need for costly, avoidable protocol amendments or site expansions.

Conduct feasibility and select sites and investigators that put your trial on the path to success

With protocols becoming more complex and an increasing number of trials competing for the same pool of patients, site and investigator selection can make or break a trial. How do you ensure that your selections are giving your trial the best chance for success?

Digital globe showcasing the reach of Citeline's intelligence platform giving clients access to clinical trial feasibility and site selection.

Sitetrove is globally recognized as the finest site and investigator intelligence platform available and, when combined with Trialtrove’s unmatched trials database, can help provide invaluable insights.

  • Make robust feasibility analysis with benchmarking available across a database of over 400,000 trials.
  • Identify sites and investigators with experience of recruiting similar patients.
  • View country selection with a high number of sites/investigators with prior experience.
  • Analyze patients being targeted by competing trials.
  • Integrate data into your own systems via API.
  • Bespoke consulting projects such as feasibility as a service, which leverages real-world data to find sites with protocol-matched patients.
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Citeline supports drug development every step of the way

Trialtrove and Sitetrove are hailed across industry as being the best resources available when it comes to protocol optimization, feasibility and site - investigator selection, but we don’t stop there – Citeline can support you at every step in the drug development journey.

From preclinical commercial and licensing, all the way through to patient engagement - recruitment and regulatory submissions – Citeline has a solution for you.

Relevant Products & Services

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Citeline SmartSolutions
Citeline SmartSolutions is an integrated suite of AI-enabled technology products that optimize and accelerate clinical trial planning and site selection.
Key Benefits
  • Recommendations on primary endpoints and I/E criteria
  • Leverage AI-enabled technology built on industry-leading Sitetrove and Trialtrove data
  • Create more predictable timelines
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Investigator SmartSelect
Harnessing the power of artificial intelligence (AI), Investigator SmartSelect combs through our comprehensive database to find the right investigators for your clinical trial.
Key Benefits
  • Generate a list of investigators in minutes
  • Reduce protocol amendments
  • Track investigator selections against your goals
Pharmaprojects
Pharmaprojects
With a comprehensive database of over 90,000 drug profiles, including 20,000 in active development, Pharmaprojects is the industry standard for tracking and analyzing the global drug R&D landscape. It serves as the trusted reference for the global drug R&D industry pipeline, offering a holistic view from preclinical to launch.
Key Benefits
  • Assess the competitive landscape
  • Support BD and licensing activities
  • Monitor vital market trends
Sitetrove
Sitetrove
Identify the sites and investigators that will help propel your trial over the line. Sitetrove’s team of expert analysts curates data from over 60,000 sources, resulting in a database that boasts over 530,000 investigators and more than 190,000 clinical trial sites spanning 185 countries.
Key Benefits
  • Successfully conduct site and investigator selection
  • Inform successful country selection
  • Get direct access to our leading expert analysts
Trialtrove
Trialtrove
Comprehensive clinical trial data you can trust. Combining unmatched coverage of the clinical trial space with unparalleled detail and granularity, Trialtrove is the only resource you can rely on to help surface the insights that will inform your strategy and enable you to deliver successful trials that meet your objectives.
Key Benefits
  • Improve your protocol development
  • Understand competitor clinical strategies
  • Get direct access to our leading expert analysts
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