Your clinical data demands precision, expertise, and innovation—and that starts with the right people. As a leading biometrics CRO, Intego Clinical provides top-tier Statistical Programmers, Data Managers, Biostatisticians, and clinical data professionals for all engagement models to help you meet and exceed industry standards.
With a foundation built on integrity and intelligence, our team stays ahead of the latest regulatory requirements, scientific advancements, and technological innovations in life sciences. We cultivate this expertise through ongoing international training, mentorship, and professional development, ensuring that every member of our extensive biometrics team brings the insight and agility needed to drive successful clinical outcomes.
Backed by a history of excellence, a commitment to quality, and proven recruitment and HR strategies, Intego Clinical is the long-term biometrics partner designed to bring you greater confidence in every data point and every decision.
We are home to the largest team of clinical data professionals in Eastern Europe
Intego is trusted as a Tier 1 strategic partner for several of the world’s top pharma companies
At Intego Clinical, we have nearly perfected the art of biometrics resourcing, ensuring that pharma, biotech, and CRO clients have direct access to exceptional Statistical Programmers, Data Managers, and Biostatisticians. Our tailored engagement models, including FSP Staff-Augmentation, Project Outsourcing, or Unit-Based offer the flexibility and expertise needed to optimize clinical programs.
This proven approach fuels our ability to scale consistently, with double-digit growth regularly achieved. Through industry-leading training programs in Statistical Programming, Biostatistics, and Data Management, we continuously expand our global capabilities, ensuring that you receive best-in-class biometrics support that evolves with your evolving needs.
We provide comprehensive end-to-end services, from Phase I to post-marketing, in all major therapeutic areas, and we comply with all regulatory global standards. Our attention to detail and willingness to problem-solve make us the ideal partner for your clinical studies.
We help our clients get the most out of their clinical data with innovative and accurate data management solutions. Our experienced data specialists are experts in various data collections and reporting systems used throughout Phase I-IV studies.
We’ve successfully brought many drugs in all main therapeutic areas to market over the years. From study conception to analysis and regulatory submissions, we help our clients get the most impact and insights from their clinical studies.
We bring software engineering talent from different industries to deliver creative solutions in the clinical setting. Our IT experts come from a variety of industries, bringing fresh perspectives to challenges in software development.
We provide a full range of analyses tailored to the specific needs of Data Monitoring Committees (DMC) in clinical trials. Our experts bring a wealth of knowledge in statistical methodology, programming, and data analysis, ensuring the safety, scientific validity, and integrity of clinical data.
We specialize in all aspects of regulatory data compliance and migration strategies. No matter the size and scope of the project, Intego Clinical can map your current or legacy data to all major CDISC formats and advise on adherence to industry standards.