Pricing
Flat fees. No per-enrollee pricing. No surprise invoices. Pick the tier that fits the study you want to run.
Express
Fastest path to a ClinicalTrials.gov NCT number.
- Observational protocol template tailored to your therapy
- ClinicalTrials.gov registration and NCT number
- One validated patient-reported outcome (PRO) questionnaire
- Secure patient enrollment portal (unlimited enrollees)
- Monthly data export (CSV)
- Principal Investigator of record (via Healing Hope International)
Standard
Protocol polish, IRB liaison, and a real PRO program.
- Everything in Express
- Customized observational protocol (not a template)
- IRB submission package + liaison to our partner IRB
- Informed consent document drafted for your study
- Up to three PRO instruments (functional status, QoL, condition-specific)
- Quarterly de-identified data analysis summary
- Protocol amendments handled as they arise
Full-Service
Registration, publication-readiness, and a press engine.
- Everything in Standard
- Post-approval press release, drafted and distributed
- Monthly study-progress newsletter to your patient list
- Publication-support kit: statistical methods, figure templates, manuscript outline
- Biannual interim analysis with PI sign-off
- ORCID / PubMed co-author linkage for your name
- Dedicated study coordinator on email and voice
Add-ons
Buy these à la carte if and when you need them. Not required.
Manuscript drafting (first author)
Our medical writer drafts a submission-ready manuscript from your registry data. You review, revise, and submit under your name.
Conference poster / abstract
Abstract and poster designed for a specific conference deadline (ASH, ASCO, AAN, etc.).
Extra PRO instrument
Add another validated questionnaire (PROMIS, FIM, WOMAC, etc.) beyond your tier's allotment.
Multi-site expansion
Add a second practice site to your registry — new site packet, IRB site amendment, training.
Patient recruitment landing page
Branded recruitment page with condition education, eligibility screener, and auto-enrollment link.
What's not included
• IRB fees. Our partner commercial IRB charges a separate initial-review fee (typically $1,500–$2,500 for an observational protocol) and a modest annual continuing-review fee. This is billed directly by the IRB; we prepare the submission and liaise.
• Journal submission or open-access fees. If you want to publish in a journal that charges an article-processing fee, that is between you and the journal.
• The clinical care itself. Beacon does not bill patients, does not run an EHR, and does not touch reimbursement. We support the observational-research layer on top of your existing practice.
Ready to pick a tier?
Start the intake form — we'll recommend the tier that fits your study and send you a proposal within one business day.
Start intake