Full-Service Statistics
You receive all statistical services from a single source and are supported from study design and sample size planning through analysis, documentation, and publication.
The benefits of working with NOVUSTAT at a glance.

CEO & Founder
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NOVUSTAT GmbH

NOVUSTAT combines scientific expertise with many years of experience in medicine, clinical research, biostatistics, and other data-driven projects. We do not simply analyze statistical questions; we classify them methodologically from the outset.
We consider the research question, data structure, regulatory requirements, and the intended use of the results together. This produces appropriate methods, reproducible analyses, and transparent documentation that stand up to publication, review, and regulated settings.
For us, statistics is not an isolated calculation step, but an essential component of scientific quality. NOVUSTAT therefore stands for technical depth, clear communication, and personal accountability throughout the project.


You receive all statistical services from a single source and are supported from study design and sample size planning through analysis, documentation, and publication.
A dedicated statistical expert who understands your field supports your project, ensuring direct communication and clear responsibilities.
We review the research question, data structure, and statistical requirements to select appropriate methods and produce robust results.
Your analyses use structured workflows and transparent documentation so results remain clear, verifiable, and reproducible.
NOVUSTAT incorporates GCP, ICH, CONSORT, and other regulatory requirements and prepares consistent, audit-ready analyses and documentation.
You benefit from more than ten years of experience and expertise gained from several thousand projects in medicine, science, and data-driven fields.
Limited involvement in study design and project strategy.
Little adaptation to study design or data complexity.
Breaks in communication and methodological continuity.
Validation and documentation are often addressed only later.
Limited experience in clinical and regulated settings.
No continuously developed technical specialization.
Dependence on individual resources for larger projects.

Statistics is incorporated into planning, structure, and objectives.
Methods and documentation are tailored to the specific project.
Clear responsibility and a consistent methodological approach.
Analyses remain transparent, reproducible, and audit-ready.
Structured consideration of GCP, ICH, and CONSORT.
More than ten years of experience across several thousand projects.
A broad expert network ensures capacity and continuity.







Statistical services follow clearly defined and documented workflows.
Analyses are implemented in a structured way and remain traceable over time.
GCP, ICH, CONSORT, and other requirements are systematically incorporated.
Methods, analyses, and results are documented clearly and transparently.
Sensitive data is handled confidentially, in compliance with the GDPR, and according to clear standards.





Medical statistics for clinical trials
from study design and sample size planning to
GCP-compliant analysis and documentation.

Biostatistical planning and modeling
with analyses in accordance with ICH, CONSORT, and GCP
for medical and pharmaceutical projects.

Medical writing for clinical trials
Study reports and regulatory documents
prepared with technical precision and transparency.

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