Phastar
Phastar is a global biometrics contract research organization specializing in data solutions, biostatistics, programming, data management, and data science. Committed to quality, innovation, and client-centric approaches, they support pharmaceutical, biotech, and medical device companies worldwide to accelerate drug development, ensure compliance, and improve human health through advanced analytics, regulatory support, and strategic partnerships.
Industries
Nr. of Employees
large (251-1000)
Phastar
London, England, United Kingdom, Europe
Products
Integrated clinical monitoring and analytics platform
A centralised platform that consolidates operational, clinical and audit data into interactive dashboards, visualisations and traceable audit trails to support review, oversight and submission readiness.
Integrated clinical monitoring and analytics platform
A centralised platform that consolidates operational, clinical and audit data into interactive dashboards, visualisations and traceable audit trails to support review, oversight and submission readiness.
Services
Statistical consulting
End‑to‑end statistical advice for study design, estimand definition, analysis planning, simulations and interpretation tailored to regulatory requirements.
Biostatistical programming
Reproducible programming deliverables including analysis datasets, tables, listings and figures for clinical study reports and regulatory submission.
Clinical data management
Design and operation of data capture, cleaning and review processes with integration to common EDC systems and audit‑ready documentation.
Data science and AI analytics
Machine learning, predictive modelling, simulation and bespoke analytics to inform recruitment, risk monitoring and decision support.
Adaptive and Bayesian design services
Design, simulation and delivery support for adaptive and Bayesian trials including prior elicitation, interim decision rules and regulatory rationale.
Regulatory submission and agency support
Preparation of submission documentation, statistical outputs and support for regulator interactions and responses.
Statistical consulting
End‑to‑end statistical advice for study design, estimand definition, analysis planning, simulations and interpretation tailored to regulatory requirements.
Biostatistical programming
Reproducible programming deliverables including analysis datasets, tables, listings and figures for clinical study reports and regulatory submission.
Clinical data management
Design and operation of data capture, cleaning and review processes with integration to common EDC systems and audit‑ready documentation.
Data science and AI analytics
Machine learning, predictive modelling, simulation and bespoke analytics to inform recruitment, risk monitoring and decision support.
Adaptive and Bayesian design services
Design, simulation and delivery support for adaptive and Bayesian trials including prior elicitation, interim decision rules and regulatory rationale.
Regulatory submission and agency support
Preparation of submission documentation, statistical outputs and support for regulator interactions and responses.
Expertise Areas
- Clinical trial design and analysis
- Biostatistics and statistical consulting
- Biostatistical programming
- Clinical data management
Key Technologies
- Bayesian statistics and prior elicitation
- Adaptive trial design and simulation
- Model‑based recursive partitioning (MOB)
- PALM trees (GLM tree methods)