Submit a RFP/RFI

Clinical Study Feasibility & Consultancy Services

Independent feasibility assessments and strategic consultancy that de-risk your clinical programme before it begins. TCR Solutions evaluates protocol viability, patient availability, site capability, competitive landscape and timelines so sponsors can make confident go/no-go decisions.

circle-icon
bottom-curve-icon
European CRO for US companies

What we deliver

  • Country and site-level feasibility questionnaires (SFQs)
  • Patient population and recruitment rate modelling
  • Competitive trial landscape analysis
  • Investigator and site capability assessment
  • Realistic enrolment timelines and risk register
  • Strategic recommendations on study design and operational approach

Why it matters

  • Avoid under-enrolling sites and missed timelines
  • Strengthen protocol assumptions before regulatory submission
  • Provide investors and stakeholders with defensible projections

FAQs

How long does a feasibility assessment take?

Typical timelines are 4–8 weeks depending on the number of countries and indication complexity.

Do you cover global feasibility?

Yes — TCR runs feasibility across UK, EU, US and emerging markets through our partner network.

UK CRO oncology clinical trials

Start the conversation

If you are considering clinical trial support as part of your development strategy, TCR Solutions would be pleased to discuss how our services could support your programme.

Contact usinfo@tcr-solutions.com