
Services
At Cota Enterprises, we provide expert clinical research support with a commitment to precision, efficiency, and client-focused solutions. As a Kansas-based company, we bring Kansas values—integrity, hard work, and a strong sense of community—to everything we do. Whether you're a startup looking to navigate the complexities of clinical trials or an established organization optimizing your research strategies, we offer customized, high-quality services tailored to your needs.

Biostatistical Analysis
Biostatistics is at the core of clinical research, ensuring that study designs and data interpretations are scientifically sound. Our biostatistical analysis services focus on study design, statistical planning, and robust data interpretation, all while maintaining strict compliance with regulatory requirements. We work closely with our clients to develop appropriate statistical methodologies, analyze clinical data with precision, and generate comprehensive reports that facilitate regulatory approvals. Our team brings a meticulous approach to trial design, adaptive methodologies, and simulations, ensuring that clinical trials yield accurate, meaningful, and reliable results. By leveraging statistical insights, we help organizations make informed decisions that enhance the credibility of their research.

Clinical Programming & Data Management
Data integrity and security are essential for successful clinical trials. Our clinical programming and data management services ensure that research data is captured, stored, and analyzed efficiently and accurately. We specialize in SAS programming, database management, and regulatory compliance, creating streamlined processes that improve data quality and reliability. Our team implements rigorous validation checks to reduce errors, ensuring that clinical trial data is both credible and submission-ready. We also provide customized solutions for regulatory submissions, ensuring that our clients’ studies meet the highest industry standards. By maintaining a structured, audit-ready approach, we help organizations maximize efficiency while minimizing risks in data handling and trial execution.


Medical Writing & Regulatory Support
Clear, concise, and scientifically accurate documentation is essential for regulatory approval and successful clinical trial execution. Our medical writing and regulatory support services provide high-quality, submission-ready documents that adhere to FDA, EMA, and global guidelines. Our experienced medical writers craft clinical study reports, investigator brochures, protocols, and regulatory submission documents, ensuring clarity, consistency, and compliance. We work closely with clients to ensure that complex scientific data is translated into accessible, well-structured reports that support approval processes and publication efforts. Whether you need assistance with regulatory submissions or scientific publications, our expert team ensures that your documentation is meticulously prepared and meets the highest industry standards.
Contact us today
At Cota Enterprises, we are more than just a service provider—we are your trusted partner in clinical research. Let’s work together to bring life-changing innovations to market.