Clinical Trial Industry

Life Science Niche Expertise

No matter your life science niche, Evoclinical can help support your clinical trial requirements.

CRO expertise you can trust

We are a Contract Research Organization with expertise that encompasses the planning and analysis of clinical trials. This includes statistical consulting, biostatistics, programming, data management, medical writing, clinical trial feasibility analysis and regulatory support services.

Additionally, we extend our capabilities to registries, diagnostics, publication support, and exploratory analyses of medical databases. We use data-mining methods suitable for “large messy data”, ensuring comprehensive support for both pharmaceutical & biotech companies and investigator-initiated studies.

Pharmaceutical Companies

Evoclinical supports pharmaceutical companies by helping design studies, write protocols, and plan data analyses that meet regulatory standards. We prepare clean, analysis-ready datasets and deliver accurate tables, listings, and figures to support study reports and submissions. We also help manage interim and final analyses, safety data, and regulatory responses.

Biotechnology Companies

Biotech companies often face tight timelines and limited resources. Evoclinical brings needed expertise to guide study design, ensure data quality, and perform analyses that meet regulatory expectations. Services include preparing submission-ready datasets, performing complex analyses, and reviewing clinical study reports to help biotech teams move faster and reduce costly errors.

Medical Device Companies

Evoclinical helps device companies design studies that meet device-specific regulatory needs, including diagnostic performance and usability. We support endpoint definitions, hypothesis testing, and data visualization. We also support regulatory submissions and provide statistical responses to authority questions, reducing delays and improving approval readiness.

Contract Research Organizations

For CROs, Evoclinical extends expert capacity without increasing internal staff. We provide flexible support across multiple studies, including statistical planning, programming, and data review. Our team helps maintain quality, meet deadlines, and reduce rework, enabling CROs to deliver consistent, reliable results for their clients.

Statistical & Data Management Services You Can Trust

Over the years, our team has worked with intention and integrity to ensure that trust and quality are not just promises, but the very foundation of who we are.

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Attributes that differentiate us

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.

Our CRO Services:

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:

What happens next?

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