Precision Medicine Module for EHR

Clinicians can order hereditary, PGx, and tumor tests directly in the EHR. The module turns the order into a lab-ready request, routes it to an external testing vendor, and tracks it through fulfillment. It can also collect the diagnosis, indication, consent, and other supporting data required for prior authorization and medical necessity review. When results return, the module stores the report in the chart and records key findings as structured data, so teams can review the case without leaving the EHR.

As the module pulls current results from external labs, it combines them with family history and patient chart data and adds the findings to the patient’s genetic profile in the EHR. It records core findings and recommended actions as structured entries, so clinicians can review prior germline and somatic results in future encounters instead of relying on scattered reports or repeat testing.

When a prescriber selects a medication, the module checks the active order against the patient’s lab-reported genotype or predicted phenotype, which are already stored in the chart. If the drug is affected, the module shows the relevant gene-drug implication, highlights dosing or drug-selection considerations, and links to approved prescribing guidance in the ordering workflow.

The module pulls tumor biomarker results from the molecular report into the patient chart, links them to the diagnosis and prior treatment history, and presents the relevant findings in the oncology review workflow. It can show biomarker summaries, treatment implications, and matched therapy options, so clinical teams can assess the case without switching between the EHR, lab portals, and standalone reports.

The module compares the patient’s diagnosis, biomarkers, and treatment history with trial eligibility criteria and local protocols, then presents likely matches in a review queue linked to the chart. It can assign referral tasks and track screening status, so teams can move from eligibility review to referral with less manual screening.

The module brings complex findings, prior results, and follow-up context into a shared review workspace for molecular tumor boards, genetics teams, and other reviewers. Teams can document decisions, assign next steps, and keep a traceable change record. The module can also release approved result summaries to the patient portal and track reclassification or follow-up actions, so teams do not have to rely on email chains or manual logs.

For one workflow in one department

We build one EHR-integrated workflow for a defined use case, such as PGx prescribing or tumor biomarker review. Scope usually includes one lab integration, one result type or result family, structured result display in the chart, and one follow-up action such as prescribing guidance, review task, or referral trigger.

For one specialty team with broader review workflows

We build a precision medicine module for one specialty team, such as oncology, genetics, or pharmacy. Apart from connecting to the EHR, this typically covers one or two lab integrations, several result types, clinician review views, patient intake or portal inputs, and task-based follow-up for care coordination.

For a cancer or genetics program across multiple systems

We build a precision medicine module that connects several workflows and adjacent systems into one environment. The module may interact with multiple labs, normalize lab-specific result formats, support shared case review, maintain an audit trail, and integrate with pathology, patient portal, CTMS, or analytics tools.

For a multi-department or multi-site rollout

We build a broader precision medicine environment for large provider organizations that need the same workflows to work across several departments or sites. The scope may cover multiple service lines, stronger governance, broader reporting, and specialized AI tools for data summarization or pre-screening.