Products

Zelthy Cell & Gene Therapy Orchestration is an application for managing the full lifecycle of cell and gene therapies from patient identification through long-term follow-up. It coordinates every stakeholder — treatment centers, manufacturers, couriers, and care coordinators — on a single platform, managing scheduling dependencies, chain-of-custody tracking, REMS compliance, and infusion logistics for therapies like CAR-T, gene therapy, and other advanced treatment modalities.

An application for pharmaceutical product authentication — including verification scanning, suspicious activity detection, and counterfeit incident management.

A continuous adherence tracking application that integrates refill data, wearables, patient-reported outcomes, and pharmacy claims to identify non-adherence risk and trigger proactive interventions.

An analytics application that transforms pharmaceutical traceability data into demand sensing, inventory optimization, stockout prediction, and channel performance intelligence.

An application for managing pharmaceutical regulatory submission pipelines — providing unified tracking, milestone management, and health authority query coordination across jurisdictions.

An application for automated data exchange with government traceability portals — including India DCTS, Brazil SNCM, Turkey ITS, and other national systems.

Zelthy Commercial Operations covers MR tools, HCP consultation platforms, sampling management, ordering portals for clinics and distributors, and patient fulfillment infrastructure. AI agents personalise HCP engagement at scale, predict reorder probability, monitor field compliance in real time, and flag adverse event mentions during detailing.

An application for automating insurance benefits investigation, prior authorization tracking, co-pay card programs, and financial assistance workflows in pharmaceutical patient services.

An AI-augmented call center application for pharmaceutical patient services with real-time compliance monitoring, automated post-call documentation, and adverse event detection.

An application for managing clinical trial registry submissions and results posting — supporting ClinicalTrials.gov, EU CTR, and other registries with deadline tracking.

An application for managing the adverse event lifecycle — from intake and assessment through regulatory reporting, signal detection, and health authority submission.

Zelthy Traceability provides end-to-end pharmaceutical supply chain execution with AI agents that detect anomalies in serialization data, predict stockouts 7–14 days in advance, monitor cold chain temperatures with predictive alerting, and automate DSCSA/FMD compliance reporting. The Distributor Management System (DMS) module covers: distributor ordering, sales data capture, temperature data capture, and track-and-trace.

A digital enrollment application for patient support programs with self-service document submission, AI-powered verification, eligibility checks, and consent management.

A configurable platform for pharmaceutical companies to manage patient support programs end-to-end — covering enrollment, adherence monitoring, call scheduling, and outcomes tracking across therapy areas and geographies.

A coordination platform for managing home delivery of medications, nursing visits, injection training, and self-administration support directly to patients outside clinical settings.

A multi-channel patient communication application that delivers personalized educational content timed to treatment milestones across SMS, email, app, and WhatsApp.

An AI assistant for pharmaceutical compliance teams — providing regulatory Q&A grounded in SOPs, document compliance scoring, SOP drafting assistance, and policy gap analysis.

An AI-powered application for monitoring regulatory guideline changes, requirement updates, precedent decisions, and their impact on pharmaceutical product portfolios.

An AI-assisted application for drafting clinical study reports — providing section-level drafting, quality review per ICH E3, cross-reference validation, and multi-stakeholder review workflows.

An application for organizing regulatory dossier content per ICH CTD structure — including document management, publishing validation, multi-stakeholder review, and submission package generation.