From chemotherapy administration and immunotherapy to buy-and-bill drug management and clinical trial compliance, our oncology billing team ensures your practice captures full reimbursement for the most complex treatments in medicine.
Oncology practices carry millions of dollars in drug inventory that must be billed, tracked, and reimbursed accurately. Between ASP fluctuations, NDC-to-J-code crosswalk errors, wastage documentation, and sequestration adjustments, the margin between profit and loss on every infusion chair is razor-thin.
Chemo administration codes (96401-96417) require precise documentation of technique (IV push, infusion, subcutaneous), timing, sequence (initial vs. subsequent substances), and concurrent vs. sequential administration. We ensure every chair minute is captured with the correct hierarchy of administration codes.
Non-chemotherapy infusions (96365-96368) for supportive care, hydration (96360-96361), and therapeutic injections follow a complex hierarchy. The first infusion hour, additional hours, sequential infusions, and concurrent infusions each have distinct coding rules. We maximize compliant capture of every infusion service delivered.
We manage the entire buy-and-bill revenue cycle — mapping NDC numbers to correct J-codes, tracking ASP quarterly updates, documenting drug wastage (JW modifier), managing biosimilar substitutions, and reconciling drug purchase costs against reimbursement to identify underwater drugs before they erode your margins.
Radiation therapy billing spans treatment planning (77261-77263), simulation (77280-77295), IMRT delivery (77385-77387), SBRT, proton therapy, and brachytherapy. Each modality has distinct professional and technical components. We ensure accurate coding across the full radiation treatment course from planning through delivery.
The rapid expansion of immunotherapy agents (pembrolizumab, nivolumab, ipilimumab) and targeted therapies has created new billing complexities around drug coding, weight-based dosing calculations, combination therapy sequencing, and irAE management coding. We stay current with every new agent approval and its billing implications.
Separating routine care costs (billable to insurance) from investigational costs (covered by the trial sponsor) is a critical compliance requirement. We implement clinical trial billing workflows that correctly identify coverage analysis determinations and prevent both underbilling of routine services and erroneous billing of research services to insurance.
Our oncology billing team includes certified coders with deep expertise in medical oncology, radiation oncology, and hematology. We understand that oncology revenue is driven by drug reimbursement and infusion chair optimization — and we treat every dollar of drug cost as a recoverable asset.
We obtain prior authorizations for chemotherapy regimens, immunotherapy, radiation courses, and high-cost supportive medications. Our team verifies benefits, calculates patient cost-sharing, and identifies financial assistance programs before treatment begins.
On treatment days, we capture every billable element — drug codes with correct units, administration codes in proper hierarchy, E/M services with modifier -25, hydration, and supportive medications. Drug wastage is documented with JW modifiers for compliance and reimbursement.
We reconcile drug purchases against reimbursements monthly, tracking ASP-based payments, contract rates, and 340B pricing where applicable. This analysis identifies underwater drugs, reimbursement trends, and opportunities to optimize your formulary for financial sustainability.
Oncology denials often involve high-dollar claims. We have dedicated appeals specialists who handle drug authorization denials, medical necessity challenges, and underpayment disputes with clinical evidence and peer-to-peer coordination to recover maximum reimbursement.
Oncology billing involves some of the most sensitive patient data in healthcare — cancer diagnoses, treatment protocols, clinical trial participation, and high-dollar drug records. Our operations adhere to HIPAA, ISO 27001, and HITRUST security frameworks with additional safeguards for oncology-specific data sensitivity.
All oncology patient records, treatment histories, and drug administration data are processed within encrypted, access-controlled systems with full audit trails. Our team undergoes specialized training on the sensitivity of cancer diagnosis information and clinical trial data.
We maintain rigorous compliance protocols for buy-and-bill drug documentation, wastage reporting, 340B program integrity, and clinical trial billing separation. Quarterly audits verify J-code accuracy, unit calculations, and NDC crosswalk integrity across your entire drug formulary.