MissionToday
To turn clinical and real-world data into evidence that regulators, payers and clinicians can rely on.
- Regulators
- Payers
- Clinicians
About Stage Analytics, a clinical data science company
Biometrics, clinical data sciences, real-world evidence and HEOR, brought together by one partner.
Who we are
Stage Analytics helps pharmaceutical, biotechnology, medical device, and healthcare organizations transform clinical and real-world data into regulatory-grade evidence through biostatistics, statistical programming, HEOR, market access research, observational studies, and advanced analytics.
We bring biometrics, clinical data sciences, real-world evidence, HEOR and market access, evidence synthesis, scientific communications and clinical operations together, so the evidence a product needs is designed, generated and communicated as one connected body of work.
- Designed
- Generated
- Communicated
At a glance
- Who we serve
- Pharmaceutical, biotechnology, medical device and healthcare organizations
- What we deliver
- Regulatory-grade evidence from clinical and real-world data
- Standards
- CDISC SDTM and ADaM, Define.xml, cSDRG and ADRG
- Submissions
- NDA, BLA, MAA and IND, with FDA and EMA support
- Practice areas
- 7 practice areas, 24 specialist services
Mission and vision
What we do for clients today, and where that work is heading.
VisionAhead
One partner for evidence across the product lifecycle, from the first protocol to market access.
- First protocol
- Evidence generation
- Market access
What we cover
Each practice area connects to the next, from clinical trial design and data capture to regulatory submissions, real-world evidence and market access.
- Biometrics & Statistical SciencesStatistical design, programming and analysis for clinical development, from the first protocol decisions to submission-ready datasets and outputs.7 services
- Clinical Data SciencesClean, validated and integrated data: clinical data management, EDC development and validation, and data engineering across clinical and real-world sources.3 services
- Real-World EvidenceReal-world evidence programs that support regulatory, medical affairs, commercial and market access decisions throughout the product lifecycle.5 services
- HEOR & Market AccessQuantifying clinical, economic and humanistic outcomes, and turning them into value strategy, economic models and HTA submissions.5 services
- Evidence SynthesisSystematic, targeted, scoping and rapid literature reviews, and network meta-analysis for payer submissions, HTA reviews and clinical strategy.1 service
- Scientific CommunicationsRegulatory and scientific writing, and publication planning that carries evidence from protocol to journal and congress.2 services
- Clinical OperationsClinical Research Associate services: monitoring visits across the site lifecycle, TMF reviews, inspection readiness and site performance monitoring.1 service
How we work
Four habits that run through every study, dataset and deliverable.
Design first
Statistical design, endpoints and sample size are settled early, so every later dataset and output has a clear basis.
Built to standards
CDISC SDTM and ADaM, Define.xml, cSDRG and ADRG, with submission compliance considered from the start.
Quality-controlled
QC programming, validation testing, reconciliation and edit checks are part of the workflow, not an afterthought.
Connected across the lifecycle
Methods and data carry from clinical trials into real-world evidence, HEOR and market access.
Frequently asked questions
Short answers about who we are and how we work.
What is Stage Analytics?
A clinical data science company that brings biometrics, clinical data sciences, real-world evidence and HEOR together in one partner.
Who do you work with?
Pharmaceutical, biotechnology, medical device and healthcare organizations.
Which practice areas do you cover?
Biometrics, clinical data sciences, real-world evidence, HEOR and market access, evidence synthesis, scientific communications and clinical operations.
How do you approach a project?
Statistical design comes first, deliverables follow CDISC standards, and QC programming and validation are part of the workflow.
Can you support a product across its lifecycle?
Yes. We cover clinical trials, biometrics, data management, regulatory submissions, real-world evidence, HEOR and market access.
Have a different question? Contact our team
Contact our team
Tell us where you are in the product lifecycle and we will outline how our biometrics, data and evidence teams can support it.
Start with what you need