A CRO focused on Statistical Analysis & Data Management
Mission
At Evoclinical, we are committed to building an innovation-driven Contract Research Organization (CRO) that stands at the forefront of the clinical research industry. To remain competitive in the age of Artificial Intelligence (AI) and the open-source revolution in pharmaceuticals, we leverage innovative technologies and automation to enhance every aspect of our service delivery.
Areas of Expertise
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.
Quality & Trust
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. By transforming research insights into actionable strategies, we effectively supports sponsors in protocol development, trial conduct, monitoring, and data analysis ultimately advancing the future of clinical research.
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.
The following key attributes helps differentiate us from other providers.
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.
A team built on experience
Providing our clients with experienced senior team members is our focus for every engagement. Worrying about junior teams or lack of senior oversight is not something our clients are concerned about when working with Evoclinical.
Defining Your Needs
One of the most common challenges we observe during the vendor selection process is the uncertainty clients face in clearly defining their needs and in truly understanding what they’re purchasing.
When it comes to statistical services, many buyers are unsure of what expertise they require or what a reasonable investment should look like. In these moments of ambiguity, trust becomes the cornerstone of every decision. Every time we recommend a statistical approach, we’re not just offering a solution, we’re standing behind it with our name and reputation.
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.