Industries

Niche Expertise

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

Comprehensive statistical services for your clinical trial niche

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.

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 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 provides expert, affordable and reliable statistical services so sponsors can reduce costs without compromising quality, compliance, or data integrity.

Deep Expertise

We provide clients with deep statistical knowledge relevant to their specific trial design, therapeutic area, and regulatory requirements, especially for complex methodologies like adaptive designs or simulations.

Quality & Compliance

We offer confidence over data credibility, adherence to regulatory standards (GCP, ICH), CDISC compliance, and overall quality assurance processes. Our results are robust and inspection-ready.

Flexibility & Scalability

Clinical trials rarely go exactly as planned. Clients need a provider who can flexibly adapt to protocol amendments, changes in scope, or unexpected data issues without excessive bureaucracy or delays.

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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Discovery Conversation

We prepare a proposal

Niche Expertise

Comprehensive statistical services for your clinical trial niche

Pharmaceutical Companies

Biotechnology Companies

Medical Device Companies