Solutions you can build in one click
Ready-made healthcare & life-science use cases across payers, providers, patients, pharma, med-device and regulators. Hit Build this and Anxya turns it into a working product.
Payer
Claims, FWA & Prior-Auth Automation
Auto-adjudicate claims, flag fraud/waste/abuse, and automate prior authorization with clinical-criteria matching.
Risk Adjustment & Predictive Stratification
HCC risk-adjustment coding, gap capture, and predictive risk stratification for care management.
Star Ratings & HEDIS Gap Closure
Track Stars/HEDIS measures, surface open care gaps, and orchestrate member + provider outreach.
Provider Network & Value-Based Analytics
Network performance, cost & quality benchmarking, and value-based contract tracking.
Speeding up prior authorization reviews
Pull coverage requirements from CMS's coverage database or your own policies, check clinical criteria against patient records and propose a determination with supporting materials for reviewer sign-off.
Supporting claims appeals
Pull together patient records, coverage policies, clinical guidelines and prior documentation to help build a stronger, faster claims appeal.
Verifying provider credentials and directory data
Look up National Provider Identifier (NPI) registry records to support provider verification, credentialing checks and network-directory accuracy.
Triaging member messages
Help member-services teams sort through a large volume of portal messages and requests, flagging what needs immediate attention so nothing is missed.
Surfacing anomalous billing patterns
Given claims data, flag outlier billing patterns worth investigator review, such as unusual code combinations or utilization spikes by provider.
Closing HEDIS/Star Ratings gaps
Analyze member-level care-gap data and draft targeted outreach — member letters, provider alerts — to close specific quality measures before the reporting deadline.
Provider / Hospital
Point-of-Care Clinical Decision Support
Evidence-based CDS with drug-interaction, dosing and guideline alerts at the point of care.
Ambient AI Scribe & Documentation
Turn a visit conversation into a structured clinical note, orders and coding suggestions.
Revenue Cycle & Denials Management
Coding accuracy, denial prediction and automated appeals to protect revenue.
Capacity, Scheduling & Patient Flow
Optimize bed capacity, OR/clinic scheduling and reduce no-shows with smart reminders.
Coordinating care and triaging patient messages
Help care teams sort through a large volume of patient portal messages, referrals and handoffs, identifying what needs immediate attention so nothing is forgotten.
Structuring clinical documentation from notes
Turn a clinician's dictated or shorthand notes into structured documentation for review — ambient-scribing support.
Coding and claims accuracy checks
Look up ICD-10 diagnosis and procedure codes and cross-check them against documentation before a claim goes out, reducing preventable denials.
Provider credentialing and verification
Look up NPI registry records to support credentialing checks, license verification and medical-staff directory accuracy.
Identifying care gaps across a patient panel
Using registry or EHR-extract data, identify patients overdue for screenings or chronic-disease follow-up and draft a prioritized outreach list.
Drafting incident and root-cause reports
Structure a patient-safety event report into a standard root-cause-analysis format, organizing the timeline and contributing factors from staff notes.
Patient
Personal Health Companion & Care Plan
A patient app that explains conditions, tracks meds & symptoms, and coaches a personalized care plan.
Care Navigator & Appointment Prep
Find the right care, prep questions for visits, and understand costs & coverage.
Remote Monitoring & Chronic Care
Log vitals from home, spot concerning trends, and alert the care team early.
Explaining lab results in plain language
With connected lab results or health records, explain what each value means in plain language, while pointing you to your clinician for anything that needs medical judgment.
Preparing questions before an appointment
Organize your symptoms, history and questions into a short list to bring to your next visit, making the most of limited appointment time.
Spotting patterns across fitness and health data
Connected to Apple Health or Android Health Connect, detect patterns across fitness and health metrics over time and put them in plain language.
Summarizing personal medical history
With connected health records, summarize your medical history and recent trends, helping you track a chronic condition between appointments.
Explaining a medical bill or EOB
Walk you through an explanation of benefits or an itemized bill, clarifying what was billed, what insurance covered and what questions to ask billing.
Understanding when a symptom needs care
Share general guidance on when a symptom may warrant urgent versus routine care, while directing anything potentially serious to a doctor or emergency services.
Pharma / Biotech
Trial Design, Feasibility & Recruitment
Protocol design support, site feasibility, and patient-recruitment matching.
Pharmacovigilance & Signal Detection
Triage adverse-event reports, detect safety signals, and draft regulatory narratives.
Real-World Evidence & HEOR
Build RWE cohorts, run outcomes analyses, and generate value dossiers for payers.
Medical Affairs & Scientific Content
Literature monitoring, MSL insights capture, and compliant scientific content generation.
GMP Manufacturing & Batch Compliance
Batch-record review, deviation/CAPA management and GMP compliance monitoring.
Real-World Evidence (RWE)
Build an RWE platform that ingests EHR, claims and registry data, standardizes to OMOP, supports cohort building, study design and HEOR/outcomes analytics, and produces FDA/EMA/CDSCO-grade evidence with 21 CFR Part 11 audit trails and privacy controls.
Digital Twin
Build a Digital Twin that unifies patient records, labs, genomics, vitals and wearables into a living model for in-silico trial simulation, synthetic control arms, dose optimization and risk prediction — consent-gated and privacy-preserving.
Drafting clinical trial protocols
Draft a clinical trial protocol that accounts for FDA and NIH requirements and follows your organization's preferred templates, policies and datasets.
Clinical trial operations
Track indicators like enrollment and site performance from trial data (e.g. Medidata), surfacing issues before they affect a trial's timeline.
Preparing regulatory submissions
Identify gaps in existing regulatory documents, draft responses to agency queries and navigate FDA guidelines.
Responding to medical information requests
Draft evidence-referenced responses to unsolicited medical-information requests from HCPs, pulling from PubMed and your approved labeling, for medical review before release.
Triaging pharmacovigilance case narratives
Review incoming adverse-event narratives, extract structured codable fields and flag cases that meet expedited reporting criteria for safety-team review.
Early-stage target and compound research
Using Open Targets and ChEMBL, identify and prioritize candidate drug targets and surface relevant bioactive compound data during early discovery.
Pharmacy
e-Prescribing & Dispensing Workflow
Digitize prescription intake, interaction/allergy checks, dispensing and label generation with an audit trail.
Inventory, Expiry & Cold-Chain Control
Real-time stock, batch/expiry tracking, reorder automation and cold-chain monitoring across the pharmacy.
Medication Therapy Management & Adherence
MTM reviews, adherence packaging, refill reminders and counselling with outcome tracking.
E-Pharmacy Storefront & Claims
Online catalog, tele-pharmacy consults, home delivery and PBM/insurance claim adjudication.
Medical Device
Device Post-Market Surveillance
Complaint handling, MDR/adverse-event reporting and field-safety signal tracking.
Design Controls & Quality (QMS)
Design history file, risk management (ISO 14971) and QMS document control.
SaMD Performance & Regulatory Pathway
Monitor Software-as-a-Medical-Device performance and map the regulatory submission pathway.
Preparing regulatory submission files
Draft sections of a regulatory submission — device description, predicate comparison, substantial-equivalence rationale — using your design history file and existing templates.
Managing CAPA documentation
Draft a CAPA record from an initial nonconformance report, structuring the root-cause analysis and proposed corrective actions to your QMS format.
Triaging complaint reports
Review incoming complaint narratives, classify them against vigilance reportability criteria and draft the initial event description for regulatory filing.
Drafting clinical evaluation reports
Assemble a Clinical Evaluation Report, pulling supporting literature from PubMed alongside your PMCF data and risk-benefit analysis, organized to your CER template.
Building payer value dossiers
Draft a reimbursement dossier and CPT/HCPCS coding guide for a new device, pulling clinical evidence and health-economic data into a payer-ready format.
Drafting field service documentation
Turn a field engineer's notes into structured service reports and a searchable troubleshooting guide for the technical-support team.
Regulator / Agency
Submission Intake & Review (IND/NDA/BLA)
Triage regulatory submissions, check completeness, and route for structured review.
Pharmacovigilance Signal Oversight
Aggregate adverse-event data, detect population-level safety signals and prioritize action.
GxP / GMP Inspection & Oversight
Plan risk-based inspections, capture findings, and track corrective actions to closure.
RWE Framework & Post-Approval Monitoring
Assess real-world-evidence submissions and monitor post-approval risk & designation programs.
Reviewing submission dossiers for completeness
Review an incoming application against the required submission checklist and flag missing sections or inconsistencies before it's assigned for full review.
Analyzing adverse event trends
Analyze aggregated adverse-event report data to identify emerging safety signals worth flagging for deeper review.
Drafting inspection findings summaries
Convert raw inspection notes into a structured findings report, with clear citations to the relevant regulation.
Reviewing promotional material for compliance
Review a draft promotional piece against labeling and advertising regulations, flagging unsupported claims or missing fair-balance language.
Comparing guidance across jurisdictions
Compare a draft guidance document against equivalent requirements in other regions and summarize where they diverge.
Summarizing registry data for public reporting
Draft the plain-language summary of registry or surveillance data intended for a public-facing transparency report.
Diagnostic Lab
Analyzing pathology images
Via a connector like Owkin's Pathology Explorer, analyze tissue images to detect cells and map tumor regions, supporting pathologist review.
Drafting result narratives and critical-value notes
Draft the interpretive narrative accompanying a complex result — like a molecular panel — and flag critical values that need immediate physician notification.
Reviewing QC trends for CLIA compliance
Given Levey-Jennings QC data, flag Westgard-rule violations or drift patterns before they affect patient results.
Preparing for CAP/CLIA inspections
Review lab SOPs and proficiency-testing records against current CAP checklist requirements, flagging documentation gaps ahead of inspection.
Drafting variant interpretation summaries
Draft a plain-language summary of a genetic result for the ordering clinician, citing ACMG classification and relevant PubMed literature for review.
Checking prior-auth requirements for molecular tests
Check a test order against CMS or payer-specific coverage criteria and draft the documentation needed to support the claim.
Clinic
Drafting visit notes and after-visit summaries
Draft a structured note and an easy-to-read after-visit summary from a clinician's encounter shorthand, ready for review before it's added to the chart.
Drafting specialist referral letters
Draft a referral letter that pulls the relevant history, medications and reason for referral from the chart, formatted to the receiving specialist's intake requirements.
Checking claims for coding accuracy
Look up ICD-10 codes and flag mismatches between documentation and the codes selected before a claim goes out.
Drafting patient reminders and follow-up messages
Draft appointment reminders, post-visit follow-ups and recall outreach for overdue preventive care, in the practice's tone and portal format.
Preparing for HIPAA and practice audits
Review practice policies and documentation samples against current HIPAA and state requirements, flagging gaps ahead of an audit.
Verifying provider credentials for payer enrollment
Look up NPI registry records to support payer enrollment and credentialing paperwork for a new provider joining the practice.
Government
Public Health Surveillance
Flag early outbreak or adverse-event signals from literature, case reports and health bulletins.
Policy Evidence Synthesis
Synthesize peer-reviewed and real-world evidence on a proposed policy or intervention for decision-makers.
National Program Monitoring
Track outcomes of government health programs (e.g. immunization, TB control) against stated targets.
Population Genomics
Analyze population-scale genomic data (e.g. Genome India, national biobanks) to inform screening policy.
Research Funding Strategy
Map research volume vs. disease burden to flag underfunded, high-impact areas for grant bodies.
Emergency Preparedness
Model resource needs (beds, therapeutics, vaccines) under different outbreak spread scenarios.
Academia
Literature Review
Screen and synthesize literature, flagging consensus, live debate and under-researched gaps.
Grant Support
Draft citation-backed background/significance sections for grant proposals.
Translational Research
Combine genomics, proteomics and clinical data (TCGA, HPA, STRING) to surface candidate biomarkers.
Trial Recruitment
Match university patient registries/biobanks against active trial eligibility criteria.
Publication Support
Check that manuscript claims are accurately supported by their cited sources.
Collaboration Discovery
Identify labs publishing on related targets or pathways to support outreach.