Clinical Trial Feasibility Analysis

Shorten your development cycles and improve operational precision.
arrow, bullet points, plum

What is Clinical Trial Feasibility Analysis

Clinical trial feasibility analysis is the process of evaluating whether a proposed study can be successfully conducted, assessing trial design assumptions, patient recruitment timelines and investigator experience. It is one of the most critical early steps in clinical development, helping sponsors avoid delays, budget overruns and flawed operational planning.

EvoClinical’s Feasibility Tool: Data-Driven Insights

EvoClinical’s feasibility tool integrates landscape analysis, study synthesis, investigator mapping, and predictive modeling into a single streamlined process. Designed specifically for the bid-development cycle, it rapidly assembles historical data and transforms it into actionable insights for trial planning.

By embedding this feasibility-scoping module into early planning, sponsors can shorten bid timelines, improve accuracy of proposals, and increase confidence in operational strategy.

Trial Landscape Analysis

-Searches public registries using defined keywords.
-Identifies existing and past studies in the same therapeutic area.
-Highlights competing or overlapping trials that could affect recruitment.

Synthesis of Study Characteristics

-Extracts design and operational details from comparable trials.
-Summarizes elements such as endpoints, study duration, and enrollment trends.
-Provides benchmarks for design planning and risk assessment.

Investigator & Site Identification

-Maps investigators and clinical sites involved in similar studies.
-Reveals where trials were conducted and who has proven expertise.
-Supports smarter, faster site selection.

Predictive Enrollment Modelling

-Uses historical trial data to forecast recruitment timelines.
-Produces realistic projections tailored to new study designs.
-Improves accuracy of operational planning and bid competitiveness.

Why Feasibility Analysis Matters

Critical in Bid Development

Sponsors must quickly estimate recruitment timelines and operational feasibility to create competitive proposals.

Identifies Investigators & Sites

Locating experienced investigators accelerates site selection and improves trial startup timelines.

Informs Trial Design

Understanding competitor study characteristics ensures designs are realistic, achievable, and regulator-ready.

Predicts Recruitment Success

Predictive modeling based on historical trials reduces uncertainty in enrollment planning.

Clinical Trial Feasibility Analysis

Why Clients Choose EvoClinical

Specialized Expertise

Focused on statistical and feasibility analysis, not generic feasibility surveys.

Operational Impact

Feeds directly into faster, stronger bid proposals.

Predictive Power

Combines registry data with statistical modeling for more accurate forecasts.

Therapeutic Breadth

Applicable across oncology, rare disease, CNS, infectious disease, and more.

Make smarter, faster decisions

At EvoClinical, we go beyond traditional feasibility by leveraging advanced tools that combine public trial registry data, landscape analysis, and predictive modeling. Our platform delivers rapid, data-driven insights into trial comparators, enrollment feasibility, and investigator networks, empowering sponsors to make smarter, faster decisions in the bid-development cycle

Contact us

Partner with a CRO you can trust.

Our process helps put you at ease when purchasing statistical services for your clinical trial needs.

We’re happy to answer any questions you may have and help you determine which of our services best fit your needs.

Our client focus:
What happens next?
1

Schedule a call

2

Discovery Conversation 

3

We prepare a proposal 

Schedule a Free Consultation