Your PI can't remember either. But they're making enrollment decisions based on it right now—along with 86 other sites across 14 countries, each interpreting your protocol slightly differently. TrialPulse eliminates protocol interpretation variability with AI-driven real-time intelligence.
Your Medical Monitor can't be everywhere. TrialPulse can.
Sites don't remember your protocol. They reviewed it once during SIV—8 months ago—while juggling 11 other studies. Since then? Memory fades. Criteria blur. Decisions get made on incomplete recall instead of protocol precision.
At a single research institution—more than any one mind can hold.
On average—plus four to nine amendments over the life of the trial.
Yet enrollment decisions against that protocol happen every day.
Wasting site budgets on ineligible patients
87 sites, 87 slightly different interpretations
At monitoring visits, when it's too expensive to fix
Sites over-exclude to 'play it safe'
Sites hesitate on borderline cases
Hoping sites 'remember better' isn't a strategy—it's how enrollment timelines fail
You can't control enrollment speed when you can't control protocol interpretation.
The average research coordinator carries the operational memory for eleven concurrent trials.
Oncology protocols now average four to nine amendments per trial—and the cadence keeps rising.
A PI has eight minutes between rooms. They cannot memorize 250 pages—and they shouldn't have to.
TrialPulse is the Protocol Intelligence Platform that transforms your 247-page static PDF into real-time, AI-driven guidance—delivered instantly to every site, at every decision point.
Think of it as a medical monitor in every coordinator's pocket—answering eligibility questions in seconds, preventing deviations before they happen, and keeping your study top-of-mind from SIV through last subject enrolled.
With TrialPulse, global studies move faster, cleaner, and with dramatically less risk. Your sites stop guessing. Your timelines accelerate. Your portfolio becomes predictable.
Coordinators don't leave the profession because of patients. They leave because of paperwork. TrialPulse takes the heaviest cognitive work—reading and re-reading protocols—off their plate.
per protocol question for a senior coordinator.
protocol cited answers.
AI parses the new amendment against the prior version and surfaces every operationally relevant change.
The right people—by role, by site, by trial—are routed the change and required to acknowledge it.
Brief comprehension checks confirm the change was understood, not just clicked.
Watch how TrialPulse AI answers complex eligibility questions instantly. Try asking about medications, lab values, or protocol-specific criteria.
The protocol-aligned answer will appear here.
Real-time guidance at every decision point. TrialPulse AI delivers protocol-aligned answers in seconds, preventing deviations before they happen.
This is just a glimpse. The actual TrialPulse platform is trained on your complete protocol and provides answers tailored to your study's specific requirements.
See TrialPulse With Your ProtocolTrial search, matching, and clinical-trial databases all store information and leave the cognition to an overloaded human. TrialPulse reads the protocol and operationalizes it at the point of decision — a different category, and the one that moves enrollment.
| Capability | Trial databases | Matching tools | TrialPulse |
|---|---|---|---|
| Search by biomarker & variant | Partial | Partial | ✓ Real-time |
| Open cohort / slot visibility | — | — | ✓ Live |
| Cited eligibility answers | — | Partial | ✓ With citation |
| Amendment detect → verify | — | — | ✓ End-to-end |
| Comprehension proof | — | — | ✓ In-workflow |
| Portfolio risk intelligence | — | — | ✓ Predictive |
Your protocol is too important to leave to memory and guesswork. TrialPulse ensures every site—across every country, through every amendment—operates from the same understanding. The result? Faster enrollment. Cleaner data. Predictable timelines.
Enterprise sponsors running global pivotal programs.
Contract research organizations managing multi-site studies.
Research institutions and their investigator networks.
Tell us a little about your study and we'll tailor the demo to your protocol.