Real World
Use Cases
Powered by SEQSTER
SEQSTER is built for the moments that matter most in drug development. When timelines are tight, data is fragmented, and patients are hard to find, SEQSTER connects the last mile of healthcare data and turns it into action.
From early discovery to post-market surveillance, our platform enables faster decisions, smarter studies, and deeper insight into the patient journey.
01
Accelerated Clinical Trial Recruitment and Screening
Enable patients to securely connect their electronic health records from multiple providers in minutes.
02
Open Patient Registries for Continuous Study Pipelines
Open, patient-centric registries that collect real-world clinical data directly from source systems, with patient consent.
03
Post-Market Real-World Evidence and Surveillance
Continuous access to clinical data after product launch, without requiring site contracts or repeated patient outreach.
04
Rare Disease and Underserved Population Research
Empower patients to self-enroll and share verified clinical records regardless of location or health system.
05
Patient Support Programs and Long-Term Outcome Tracking
Patient support and monitoring that continuously updates medical histories and outcomes over time.
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Accelerated Clinical Trial Recruitment and Screening
Identifying the right patients is time-consuming, and medical records are incomplete or unavailable. SEQSTER enables patients to securely connect their electronic health records from multiple providers in minutes. Sponsors and their research teams gain instant access to structured, longitudinal medical histories that can be queried against inclusion and exclusion criteria in real time.
Sponsors move faster with confidence, enrolling the right patients earlier while reducing operational burden across sites and CROs.
patients before site referral
of potential participants
manual chart review
from years to months
Open Patient Registries for Continuous Study Pipelines
One-off studies limit learning and slow future programs. SEQSTER supports open, patient-centric registries that continuously collect real-world clinical data directly from source systems, with patient consent.
Sponsors build living data assets that fuel present and future trials while delivering meaningful value back to patients.
data across a portfolio
patients across multiple studies
studies as eligibility changes
progression and care patterns
Post-Market Real World Evidence and Surveillance
Long-term safety and outcome tracking is resource-intensive and incomplete. SEQSTER provides continuous access to real-world clinical data after product launch, without requiring site contracts or repeated patient outreach.
Sponsors gain a clear, ongoing view of how therapies perform in the real world, supporting both regulatory obligations and scientific insight.
multiple years
visits, outcomes, and events
and regulatory reporting
retrospective data retrieval
Rare Disease and Underserved Population Research
Patients are geographically dispersed and data is difficult to aggregate. SEQSTER empowers patients to self-enroll and share verified clinical records regardless of location or health system.
Sponsors uncover insights that would otherwise remain hidden, accelerating research in areas with the greatest unmet need.
data across a portfolio
patients across multiple studies
studies as eligibility changes
progression and care patterns
Patient Support Programs and Long-Term Outcome Tracking
Maintaining sustained engagement and visibility outside traditional clinical trial settings is challenging, such as in Risk Evaluation and Mitigation Strategy (REMS) registries. SEQSTER supports patient support and monitoring programs by continuously updating medical histories and outcomes over time.
Programs become more scalable, more patient-centric, and more informative across the full lifecycle of care.
burden for support teams
for both patients and sponsors
through transparency and access
