Drug Development Data Intelligence

Accelerating Analysis Data for the Entire Trial Lifecycle

Analysis-ready Analysis datasets generated on demand — supporting clinical trials, safety and pharmacovigilance, PK analysis, HEOR and real-world evidence, and companion diagnostics.

Request Demo Explore Solutions

Analysis data that moves at the speed of the question being asked

New clinical data arrives continuously. Analysis-ready Analysis datasets should too. Jetacor automatically generates and refreshes Analysis datasets continuously — so clinical, safety, PK, HEOR, and companion diagnostic teams always have current analysis data on demand.

Request Demo

What Jetacor Makes Possible

Every team that depends on Analysis data — analysis-ready, on demand

Jetacor generates Analysis datasets from the latest SDTM extraction and the organization's own Analysis specification. Whether the downstream need is a clinical safety review, a PK NCA run, a pharmacovigilance signal assessment, an outcomes research analysis, or a biomarker subgroup for a companion diagnostic, the generation step is the same — upload the extraction, run against the spec, receive analysis-ready datasets immediately.

Request Demo

Generate Analysis datasets from any new SDTM extraction without manual re-programming — the same derivation logic applied every time, across every function.
Conformance checks and dataset validation reports produced automatically with every generation run.
All derivations, population flags, and variable attributes trace directly to the organizational specification that defined them.

Solutions

One platform. Every function that depends on Analysis data.

Jetacor serves every team in pharmaceutical, biotech, and CRO organizations that depends on analysis-ready data — from clinical trial monitoring and safety signal detection, to PK analysis, health economics and outcomes research, companion diagnostic submissions, and validation for regulatory submission. One platform, analysis-ready data generated automatically on every new extraction.

Request Demo

Clinical Trials

Continuous Analysis dataset generation across the trial lifecycle — from enrollment to submission

Clinical data teams depend on analysis-ready Analysis datasets for safety reviews, interim analyses, ongoing monitoring, and final regulatory submission. When a new SDTM extraction is available, Jetacor generates updated Analysis datasets immediately — applying the organization's derivation logic consistently across every data cut. Clinical teams review current data, not a weeks-old snapshot, and the same logic applied to the Week 4 cut is applied identically to the Week 12 cut and the final submission package.

Safety & Pharmacovigilance

Analysis datasets for signal detection, periodic safety reports, and expedited safety review

Safety teams and pharmacovigilance groups rely on ADAE, ADLB, ADCM, and other analysis domains to support adverse event analysis, signal detection, PSUR/PBRER preparation, and expedited safety reporting. When new safety data is received, the review cannot wait days for Analysis data to be manually generated. Jetacor generates the required safety Analysis domains from the latest extraction immediately — so safety assessments are based on what was actually collected and reported, not a stale dataset.

Pharmacokinetics

PK Analysis datasets generated from SDTM concentration and parameter domains

PK teams need ADPC and ADPP datasets for non-compartmental analysis, PK/PD modeling, dose-exposure-response evaluation, and regulatory PK reporting. Generating these datasets from SDTM PC and PP domains requires applying derivation logic that handles nominal versus actual timepoints, parameter derivation, concentration flagging, and analyte-specific rules. Jetacor generates PK Analysis domains from the organization's PK specification — so NCA and modeling workflows start as soon as concentration data is extracted, without waiting on the programming queue.

HEOR & Real-World Evidence

Analysis datasets for outcomes research, comparative effectiveness, and payer evidence

HEOR and real-world evidence teams working with RWD sources — claims data, registries, and EHR data structured to SDTM — need Analysis datasets for comparative effectiveness analyses, cost-effectiveness modeling, and payer value dossiers. Jetacor applies Analysis data derivation logic to RWD-derived SDTM, generating analysis-ready outcomes datasets with full traceability from source data to analytical results. The same platform used for interventional trial Analysis dataset generation applies to RWD programs without reconfiguration.

Companion Diagnostics

Biomarker and CDx analysis datasets generated alongside the clinical trial Analysis dataset package

Companion diagnostic and precision medicine programs require Analysis datasets for biomarker subgroup analyses, CDx analytical performance data, and regulatory submissions supporting diagnostic device approvals alongside the therapeutic NDA or BLA. Jetacor generates biomarker Analysis domains — including ADIS, ADTR, and custom biomarker and molecular response domains — from SDTM extractions that include translational and molecular data. CDx teams receive analysis-ready biomarker datasets as part of the same generation run that produces the clinical trial Analysis dataset package.

Platform Capabilities

Everything Research Teams Need in One Workflow

Analysis Dataset Generation

Generate analysis datasets from clinical data extractions across clinical trial, safety, PK, HEOR, and companion diagnostic programs — driven by the organization's own derivation specification.

Analysis Specification Authoring

Author and maintain analysis specifications from the clinical data domain inventory — the single source of truth that drives every generation run and ensures derivation consistency across all programs.

Regulatory Submission Analysis Dataset Validation

Validate generated analysis datasets against regulatory submission standards — automated conformance checks and structured validation reports produced with every generation run, ready for independent review.

Every analysis — whether for a safety signal review, a PK NCA run, an outcomes research model, a biomarker subgroup for a companion diagnostic, or the final regulatory submission package — depends on Analysis data. Making that data available on demand, consistently, from the latest SDTM extraction, changes what teams can do and when they can do it.

Jetacor

Request a Demo

See Jetacor in action

Submit the form and the Jetacor team will reach out to schedule a demonstration. Organizations that want to validate the platform against their own data and standards can be onboarded for platform access after the demo.

Privacy Policy — Jetacor is operated by Jetacor. Files and data uploaded during a session are used solely for processing the requested output and are not stored beyond the active session. Personal health information and clinical trial data are not collected, retained, or shared. By using this platform, users agree to these terms.

Accelerating Analysis Data for the Entire Trial Lifecycle

Analysis data that moves at the speed of the question being asked

Analysis Data on Demand

Tailored to Organizational Standards

One platform. Every team. Every question. Always analysis-ready.

Every team that depends on Analysis data — analysis-ready, on demand

One platform. Every function that depends on Analysis data.

Everything Research Teams Need in One Workflow

See Jetacor in action