Services

Clinical Trial Statistical Services

Transforming research insights into actionable strategies you can trust

At Evoclinical, we are committed to building an innovation-driven Contract Research Organization (CRO) that stands at the forefront of the clinical research industry.

Comprehensive clinical trial statistical services you can trust

Our areas of expertise encompass the planning and analysis of clinical trials, statistical consulting, biostatistics, programming, data management, and medical writing, supported by robust software experience in data science and registry-centric data mining technologies. 

Additionally, we extend our capabilities to registries, diagnostics, publication support, and exploratory analyses, ensuring comprehensive support for both pharmaceutical & biotech companies and investigator-initiated studies.

WHAT WE PROVIDE

Services

Statistical Consulting

We can provide clinical trial design and statistical advice and guidance in short order. Be it interpreting concerns from a regulatory authority, endpoint selection, efficient study design features, handling intercurrent events, cost and timeline reduction, or providing Competitive Landscape Analysis, to name but a few.
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Statistical Analysis

Evoclinical provides statistical services for clinical trials, including analysis plans, CDISC-compliant data sets, tables, listings, figures, randomization setup, interim and final analyses, safety summaries, integrated safety and efficacy summaries, clinical study report reviews, and full submission support.
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Clinical Study Design

New product indication, target population, mechanism of action, and regulatory pathways are used to research and recommend study design options that will efficiently answer research questions while meeting regulatory requirements and expectations and business constraints.
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Regulatory Services

Evoclinical supports regulatory submissions by preparing data packages, TLFs, and briefing materials. Statisticians join sponsor teams to answer authority questions, attend meetings, draft responses, and ensure study designs meet regulatory standards. Their expertise helps sponsors avoid flawed designs and keep preferred study options open.
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Data Management

Evoclinical’s data management team supports clinical trials with eCRF setup, testing, and training, logic checks, query handling, medical coding, and data review. They manage study metrics, database locks, lab ranges, and site support to ensure data are accurate, complete, and analysis-ready while meeting regulatory and protocol requirements.
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Statistical Training

Evoclinical offers custom statistical training to help sponsor teams better understand clinical research statistics. Topics to consider are protocol writing or interpretation, purpose and benefit of study design features, analytical methods like hypothesis testing and missing data adjustment methods, and results interpretation.
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Medical Writing

Evo Clinical medical writers are qualified to write documents for submission to regulatory authorities, e.g., study protocol, clinical study reports, informed consent forms.
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Competitive Landscape Analysis

De-risk study design and shorten start-up timelines! Our clinical trial landscape analysis toolset instantly converts global registry data into dashboards that benchmark protocols (i.e., key trial characteristics including sample size, phase, number of sites, etc.), pinpoint top investigators, and optimize site selection.
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Quality Matters

Evoclinical prioritizes quality through a dedicated quality management system, in-house software validation, and rigorous risk-based monitoring, ensuring that all deliverables meet the highest standards.

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Partner with a CRO you can trust.

Our process helps put you at ease when purchasing statistical services for your clinical trial needs.

We’re happy to answer any questions you may have and help you determine which of our services best fit your needs.

Our client focus:
  • Client-oriented
  • Deep Expertise & Experience
  • Data Quality & Compliance
  • Flexible & Adaptable
  • Results Oriented
  • Cost - Effective
What happens next?
1

Schedule a call

2

Discovery Conversation 

3

We prepare a proposal 

Schedule a Free Consultation