Observational Research, Simplified
The modern approach to observational research, harnessing cutting-edge technology to tackle your toughest questions and uncover the insights you need.
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Published with the biggest names in life sciences
Why life science leaders choose PicnicHealth
30%-50% more cost effective than a traditional site-based model.
Study kickoff to first-patient-in in less than 3 months, recruitment as fast as 4 months, and participant data available days after enrollment.
98% patient retention year-over-year. Patients are recruited based on your study needs and FDA diversity mandates.
Real-time visibility and transparency into every aspect of the study. Access to deep comprehensive patient data to understand your population and adapt your study at any time to your changing needs.
A direct relationship with patients that enables us to capture medical records across all sites of care and collect PROs and other patient-generated data with ease.
Run virtual or hybrid studies. With any study design, remove all the unnecessary work from sites that they don’t want to be doing.
Start with a consented patient
Patients join studies on the PicnicHealth platform.
Retrieve the data
Retrieve medical records from any site of care across the U.S. to create the Universal Patient Record.
Ongoing data collection
Continue to follow the patient and keep them engaged over time with our patient app.
PicnicHealth by the numbers
Patients are at our core
Our AI health assistant, powered by the Universal Patient Record, supports patients and enables them to contribute to research from home.
Explore the Patient AI AssistantNear real-time visibility into your study's progress
Track recruitment progress, view response rates to clinical assessments, and monitor emerging trends in your data. PicnicHealth takes care of the rest.
Explore our Sponsor Portal
PicnicHealth supports life sciences customers across use cases
Get the endpoints you need, faster and more easily.
Access complete data for more informed decision making.
Build a body of real-world evidence around your target disease or drug.
Demonstrate utilization and value to all stakeholders.