De-risk your strategy before you commit
Choose the right countries, sites, and CRO with confidence.
$1.6M saved on amendments in one Q
3x faster recruitment
25% less time of country feasibility
One System. Every Decision From Market Research to CRO Selection.
Validated, current, and traceable—a glassbox data experience.
Validate your product before you invest.
Find the markets that need your treatment.
- Compare your therapy against regional treatment standards to make sure you’re addressing unmet clinical needs.
- Predict commercial viability and the potential impact of your therapy.
- Enhance your product development strategy with accurate, data-driven insights for a better market position.
“When we are pulling together a strategy, we like to be able to compare the asset we’ll be investigating to the SoC in that country. It gives us a better idea how investigators will receive the protocol.”
Stacy Weil
Senior Vice President, Patient Centricity and Business Operations, Premier Research
“Standard of care speaks to the eligibility of a patient. If a SoC drug renders a patient ineligible to participate in the study, that’s going to impact our recruitment and timelines.”
Annie Rotten
Manager, Strategic Site Solutions, Avance Clinical
Build a protocol grounded in real clinical practice.
To serve real patients, not theoretical models.
- Design realistic, practical trial protocols that align with local treatment practices.
- Ensure control arms accurately represent existing reimbursed treatments based on Standard of Care benchmarks.
- Assess patient burden, site capacity, and endpoint suitability with in-depth Standard of Care insights.
We helped Boehringer Ingelheim turn patient insights into actionable data.
Here’s what they said about our partnership:
TrialHub enables a rapid translation of expansive datasets into actionable patient-centric insights, reducing the time needed for analysis from 3-6 months to several hours.
Judge a CRO by their site selection, not their pitch
Verify site quality and trial performance yourself, before you commit.
- Use accurate, unbiased data on trial performance, country, and site capacity to compare study strategies and choose the best fit.
- Align your country and site selection with the unique needs of your indication and patient population.
- Stay ahead of risks by tracking shifts in the landscape and ensuring your CRO’s strategy continues to serve your trial’s needs.
“We’ve been able to partner with our clients—small biotech and pharma—and give them realistic enrollment projections.”
Curtis Head
Co-founder and CEO, PRC Clinical
“TrialHub helps us find out if a study will be successful and provides robust data to back it up.”
Stacey Collins
Director, Study Start-up and Feasibility, Bionical Emas
Submission timelines and real-world regulatory nuance
- Compare country-specific submission timelines.
- See the factors that actually move your timeline: ethics committee models, import permits, language requirements.
- Get instant answers from TrialHub’s AI Regulatory Assistant instead of another round of manual searches.
Expert Support
You don’t need a big internal team.
With Ask the Analyst, TrialHub’s medical team becomes yours.
Annie Rotten
Manager at Avance Clinical
Jessica Rouet
Business Development Associate EAP, Bionical Emas
Andreas Beust
President, AICROS
Mid-sized
CRO
Mid-sized
CRO
Mid-sized
CRO
- Dedicated team of medical experts, analysts and data scientists just one click away.
- Exceptional, human customer support at every step of the way.
- A product roadmap developed with your needs in mind.
Get Started
We’re here to help your product reach patients faster
Don’t waste years in delays. Patients need innovative treatments now.