The Safest and Most Compliant Generative AI Agents for Life Sciences
Proving clinical abundance across the BioPharma & MedTech value chain
Trusted by the Top 5 Pharma
& Over 50 Global Healthcare Partners
Life Sciences Use Cases Powering Clinical Abundance
Clinical Trials
Participant Prescreening
Prescreen for eligible participants, assess fit against multiple trials, and accelerate enrollment timelines.
Clinical Trials
Informed Consent Education
Guide participants through consent, explain study expectations, and confirm understanding before enrollment.
Clinical Trials
Visit Coordination
Remind participants of visits and procedures, explain preparation steps, and reduce missed appointments.
Clinical Trials
Participant Follow-Up and ePRO
Monitor symptoms, collect study updates, and escalate potential safety issues between visits.
Clinical Trials
Study Support for PIs
Clinical Trials
Patient Support
Patient Assistance Program Enrollment
Screen patients for eligibility, explain available financial assistance options, and support enrollment through approved workflows.
Patient Support
Therapy Onboarding
Deliver approved educational content, reinforce appropriate product use, and support patients during therapy initiation.
Patient Support
Insurance & Reimbursement Support
Verify coverage, assist with benefits investigation and prior authorization, and route patients to reimbursement solutions.
Patient Support
Pharmacy Access Coordination
Confirm product availability at local pharmacies and guide patients to alternate access pathways when needed.
Patient Support
Adherence and Refill Outreach
Proactively remind patients of refills, confirm pharmacy fulfillment, and address access barriers impacting adherence.
Patient Support
HCP Engagement
PSP/PAP Program Updates
Educate HCPs on patient support/access programs (PSP/PAP), share product/program updates, and provide updated resources.
HCP Engagement
Coverage & Affordability Support
Answer reimbursement and prior authorization questions, triage benefits issues, and help resolve coverage barriers to therapy.
HCP Engagement
Product Education
Provide approved clinical education (dosing, safety, administration) and respond to product-specific questions
HCP Engagement
Patient Journey Navigation
Help HCP offices navigate next steps for patients, referrals to support services, onboarding to programs, reminders/ follow-ups, and connecting to appropriate channels for additional help.
HCP Engagement
Adverse Event Intake & Escalation
Collect detailed adverse event reports from HCPs, confirm required details, and escalate appropriately per pharmacovigilance processes.
HCP Engagement
Life Sciences Executive Advisory Panel
Jim previously served as EVP and Chief Commercial Officer at Gilead, where he oversaw the launch of 24 products, including 11 brands with peak annual revenues exceeding $1 billion, as well as the two most successful launches in pharmaceutical history as measured by first-year revenue. Jim began his career at Stuart Pharmaceuticals (Zeneca), a predecessor to AstraZeneca.
Jim Meyers, Former Chief Commercial Officer at Gilead Sciences
Michael Norton , Former Head of Global Medical Affairs at AbbVie
Jessica currently serves as SVP and Global Head of Quality, Research and Development at Takeda. Previously, she was SVP and Global Head of Medical Affairs, Clinical Affairs, HEOR, and Regulatory Affairs at Philips. She spent nearly 20 years at Johnson & Johnson, most recently serving as SVP, Global Medical Device Sector Lead for Preclinical, Clinical Medical Strategy & Operations.
Dave Pierce previously served as EVP and President of the MedSurg, Endoscopy, and Urology businesses at Boston Scientific. Over his 30-year tenure, he guided the company’s commercialization, market access, and clinical adoption of device innovations. During this period, Boston Scientific evolved into one of the world’s largest medical device companies, with annual revenue rising to approximately $20 billion.
Dave Pierce, Former President, MedSurg, Endoscopy, and Urology at Boston Scientific
Proven Results in Life Sciences
Clinical Trial Prescreening
Increase in qualified on-site screening appointments.
Multilingual Outreach
2.6X
276%
<3%
Refusal rate with high-trust engagement across programs.
Evaluation Framework Built for Life Sciences
We’re the only company that performs output testing on our LLMs. We hired over 7k U.S. licensed clinicians to make over 500k test calls. Our team of experts conduct additional compliance evaluations.
