As a full-service CNS CRO, we combine deep, indication-level expertise, 25+ years of global experience, proven processes, and the latest technology to move your CNS clinical development program forward.
Clinilabs’ specialty focus enables us to prioritize projects that large CROs cannot. For sponsors and projects of all sizes, we work to ensure that the “A team” we present before the award is the same team that supports your project after the award is made. Our senior management is involved in every project we manage, ensuring that your project receives attention at the highest level of our organization.
Your Pathway to CNS Approval
Clinical Development Pathway
We set your CNS clinical trial up for success from the start, with smart strategies for regulatory application, trial design, subject selection, and outcome assessments tailored specifically for your study.
Our network of high-performing, CNS investigators ensures that you meet enrollment targets and achieve milestones fast — without sacrificing data quality. Our Accelerator Site program, which includes top-rated sites worldwide, guarantees that critical milestones will be met on time, every time.
Our integrated clinical data management solutions utilize the latest in digital technology, applying eTMF, eCRF, and eSource to streamline data handling, monitoring queries, and biostatistics. Our proprietary application, Clinical InSite™, collects and consolidates data from integrated sources, integrating the data with your clinical database.
CNS specialty services, such as our placebo response management program, minimize variability in datasets, enabling you to detect differences between active drug and placebo when such differences exist. Other CNS specialty services, including CNS biomarkers, offer the value only available from a CNS specialist.
Our agile, built-in clinical trial management services, dedicated project leads, and high-touch communication minimize friction and keep your trial on track. We manage by working with you to create a unified clinical development team, so our organization and yours function as one.
Data quality and compliance are critical to our mission, ensuring that we produce audit-ready, perfected data for your drug or medical device submission. Our experience with regulatory authorities in North America, Europe, and Asia allows you to undergo regulatory inspections with confidence.
We set your CNS clinical trial up for success from the start, with smart strategies for regulatory application, trial design, subject selection, and outcome assessments tailored specifically for your study.
Our network of high-performing, CNS investigators ensures that you meet enrollment targets and achieve milestones fast — without sacrificing data quality. Our Accelerator Site program, which includes top-rated sites worldwide, guarantees that critical milestones will be met on time, every time.
Our integrated clinical data management solutions utilize the latest in digital technology, applying eTMF, eCRF, and eSource to streamline data handling, monitoring queries, and biostatistics. Our proprietary application, Clinical InSite™, collects and consolidates data from integrated sources, integrating the data with your clinical database.
CNS specialty services, such as our placebo response management program, minimize variability in datasets, enabling you to detect differences between active drug and placebo when such differences exist. Other CNS specialty services, including CNS biomarkers, offer the value only available from a CNS specialist.
Our agile, built-in clinical trial management services, dedicated project leads, and high-touch communication minimize friction and keep your trial on track. We manage by working with you to create a unified clinical development team, so our organization and yours function as one.
Data quality and compliance are critical to our mission, ensuring that we produce audit-ready, perfected data for your drug or medical device submission. Our experience with regulatory authorities in North America, Europe, and Asia allows you to undergo regulatory inspections with confidence.
Complete CNS CRO Solutions
CNS clinical trials are more complex than trials in other therapeutic areas. They may have more, or more challenging, inclusion/exclusion criteria, employ subjective and rating-scale-dependent assessments, be impacted by placebo response, and fail more often than trials in other therapeutic areas. This is why specialty expertise is critical to success.
When you work with Clinilabs, you’re not just getting a generalist CRO; you’re getting a specialty partner with expertise and skill sets that are fully aligned with your needs. We are committed to using the experience we’ve gained in over 25 years and more than 800 clinical trial projects to apply the best people, processes, and systems to meet the specific needs of your clinical trial. We don’t rest until every aspect of your trial is optimized for success.
CNS Clinical Trial Expertise
Clinilabs is your full-service CRO focused on CNS drug, device, and technology development. Driven by a passion to bring new therapies to patients living with mental health, neurological, and substance use disorders, our CNS experts don’t just manage CNS clinical trials — we supercharge them.
