An application for organizing regulatory dossier content per ICH CTD structure — including document management, publishing validation, multi-stakeholder review, and submission package generation.
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.
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.
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.
An application for managing multi-tier pharmaceutical distribution — including secondary sales tracking, channel inventory monitoring, trade scheme management, and redistribution alerts.
An application for pharmaceutical product authentication — including verification scanning, suspicious activity detection, and counterfeit incident management.
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 continuous adherence tracking application that integrates refill data, wearables, patient-reported outcomes, and pharmacy claims to identify non-adherence risk and trigger proactive interventions.
A coordination application for nurse educators managing patient assignments, visit scheduling, documentation, and outcomes reporting in pharmaceutical support programs.
An application for automated data exchange with government traceability portals — including India DCTS, Brazil SNCM, Turkey ITS, and other national systems.
An analytics application that transforms pharmaceutical traceability data into demand sensing, inventory optimization, stockout prediction, and channel performance intelligence.
An application for managing clinical trial registry submissions and results posting — supporting ClinicalTrials.gov, EU CTR, and other registries with deadline tracking.
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.