Panacea helps doctors and health systems identify which patients may benefit from Whole Exome Sequencing, order testing through accredited labs, and deliver results and follow-up at scale, without building a genetics program from scratch.
Actionable genetic risks for cancer, cardiovascular disease and more often go undetected until it’s too late to prevent them. The barrier usually isn’t the test. It’s everything around it.
Applying genetic testing guidelines takes specialized knowledge and time most visits don’t have.
Many physicians were never trained to order, interpret or discuss genomic results with confidence.
Delivering results, counseling and follow-up to hundreds or thousands of patients is an operational problem, not just a clinical one.
When a hereditary risk is found, relatives who share it rarely get notified or tested.
One platform from patient intake to family follow-up. Your physicians stay in control of every clinical decision.
A brief questionnaire on personal and family history, completed online before or after a visit. No extra appointment time.
Responses are checked against clinical guidelines across cancer, cardiovascular, neurological and rare disease, and summarized for the physician.
The physician reviews the summary, talks with the patient and orders Whole Exome Sequencing through our CAP- and CLIA-accredited lab partner.
Physicians get a clear report with guideline-based next steps. Patients get their own portal, a genetic counseling session and tools to notify family members.
Add genomic prevention to your membership without hiring genetics staff. Panacea supplies the guideline expertise, lab, counseling and patient experience.
Whether you’re identifying candidates or moving toward population-scale testing, Panacea handles intake, results delivery and follow-up across departments.
Give your clinicians a ready-made genomics workflow that fits a virtual model, from online intake to at-home sample collection.
Software, lab testing and genetic counseling in one partnership.
Candidacy summaries, ordering and results in one place, with interactive guides for first-time users.
Patients complete forms, track their kit and review results in plain language.
Every known gene sequenced through an accredited lab partner, with raw data available on request.
A post-test session with a certified genetic counselor is included with every test.
Ready-to-send notifications help patients tell relatives who may share their risk.
HIPAA compliant platform
See Panacea working with your own physicians and patients before committing. Pilots run on our standalone platform, so there’s no IT integration project to get started.
We set up your practice and train your physicians and staff.
Your team uses the full workflow, from survey to results and follow-up.
We review outcomes together, and the pilot converts to an annual license.
Preventive WES is rarely covered by insurance, so most practices offer it as a patient-pay service. HSA and FSA are accepted.
Your physicians, always. Panacea organizes patient history against published guidelines; the physician decides whether to test.
That’s who we built it for. Guided onboarding, report walkthroughs and included genetic counseling support every step.
Pilots run for six months with a modest fee and convert to an annual platform license. We’ll tailor the scope to your organization.
Tell us about your organization and we’ll set up a walkthrough of the platform and pilot options.
Prefer email? contact@seekpanacea.com