Make patient assistance paperwork easier to complete and track.

The problem we exist for

Manufacturer patient assistance programs can make medication available at no cost to eligible patients, but practices often manage enrollment through manufacturer-specific forms, signatures and supporting documents. Staff may re-enter the same patient information across applications and renewals, then track submissions across separate portals, faxes and spreadsheets. Patient signatures, incomplete documentation and approaching renewal dates can all delay the process.

A patient may qualify for help and still face an administrative barrier to completing the application.

What we do

• Resolve the correct current manufacturer form for a medication, including variant forms that depend on indication.
• Fill it from the practice’s own records, chart, prescriber profile, insurance on file and prior applications, with the provenance of every value visible.
• Collect the patient information and signature through a portal invite or a single-use, identity-verified link sent by text message, with no account required for a signature-only request.
• Assemble and deliver the submission packet, and track it through to a decision.
• Open renewals ahead of expiry, reusing verified data, and require a fresh, explicit decision on every optional program enrollment rather than carrying one forward.

What we deliberately do not do

This list matters more than the one above, because it is the list a practice can hold us to.

• We do not determine eligibility. Manufacturer programs set and assess their own criteria. We do not predict approval or claim to improve the odds of a decision.
• We do not publish eligibility numbers we cannot source. Income limits and program terms change, so every figure lives on the manufacturer’s own page, which is where our guides link.
• We do not host or mirror manufacturer forms. Every guide links out to the manufacturer’s official program page instead.
• We do not imply partnership with any manufacturer. We are not affiliated with, endorsed by, or sponsored by any of them, and we do not use their logos.
• We do not infer consent. Optional manufacturer enrollments and communications require a fresh, explicit decision every time. A prior copay or quick-start decision never becomes standing consent for a later program.
• We do not upgrade our compliance language. "HIPAA-aligned architecture, BAA available" is what we can evidence, so it is what we say.

How to check any of this

Ask for the customer security FAQ, the data-flow and boundary document, and the evidence checklist. Ask what our current attestations actually cover. Ask whether a relevant customer reference is available, and compare written answers with the current evidence provided during diligence. Oureditorial methodology explains how the program guides are sourced, reviewed and kept current.

The numbers, and where they come from

These figures can change with a release. If one appears outdated, contact us so we can verify and correct it.