Statistical Analysis, Biostatistics & Data Management for Clinical Trials

Turning Clinical Data into Smarter & Faster Decisions

Focus

Biostatistics & Data Management

20+

Years

Average Trial experience

10+

Areas

Therapeutic areas

Statisticians hold PhDs

200

Studies Supported

SERVICES WE PROVIDE

Biostatistics & Data Management for Clinical Trials

Statistical Consulting

We provide 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.

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 submission support.

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.

Regulatory Support Services

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

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. We 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.

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.

Why us

Why clients work with
EvoClinical?

Cost-effective

Evoclinical leverages Ai capabilities to help provide affordable and reliable statistical services & Data Management services so sponsors can reduce costs without compromising quality, compliance or data integrity.

Deep Expertise

We provide clients with deep statistical & data management knowledge relevant to their specific trial design, therapeutic area, and regulatory requirements, especially for complex innovative designs.

Quality & Compliance

We instill confidence in data integrity through adherence to regulatory standards (ICH), industry standards like CDISC, and overall quality control processes. Our results are robust and inspection ready.

Flexibility & Scalability

Clinical trials rarely go exactly as planned. EvoClinical flexibly adapts to protocol amendments, changes in scope, or unexpected data issues without excessive bureaucracy or delays.

Partner with a BioStatistics CRO you can trust.

Our process helps put you at ease when purchasing statistical services

Whether you’re facing a mid-program regulatory change, complex study design questions, or need transparent statistical methodology that can withstand regulatory scrutiny, EvoClinical’s biostatistics team is ready to help.

Focus areas:

What happens next?

Schedule a call

Discovery Conversation

We prepare a proposal

Schedule a Free Consultation

Certifications & Affiliations

We offer confidence over data credibility, adherence to industry certifications and overall quality assurance processes.