Contract Research Organization
We conduct research in the Russian Federation and the EAEU countries
- EN
- RU
K-Research is a contract research organization (CRO) that has been successfully operating since 2018, offering a comprehensive range of services for conducting Phase I-IV clinical trials across the Russian Federation and several countries within the Eurasian Economic Union (Armenia, Belarus, Kazakhstan).
We are a trusted partner in the field of clinical research, providing end-to-end support from study planning and design to data collection and analysis.
Professionals with extensive experience in pharmaceutical companies and global CROs.
Most of our CRAs hold medical degrees and have over two years of experience in clinical research. Located across multiple cities, they help optimize monitoring visit costs for our clients.
Proficient in creating and reviewing clinical trial documents, including protocols, informed consent forms, safety reports, and clinical study reports.
Over the past few years, our regulatory specialists have successfully secured numerous approvals from regulatory authorities in both Russia and other countries.
Specialists are experts in working with Russian electronic case report forms (eCRFs) and possess extensive experience in handling data for both small-scale Phase I studies and large-scale patient registries.
Experts in developing statistical analysis plans, conducting data analysis, and preparing statistical reports for clinical trials.
Our team conducts full-cycle clinical trials across all phases within the Russian Federation and EEU countries, ensuring exceptional data quality and compliance with regulatory standards. We have extensive expertise in therapeutic areas such as oncology, hematology, gastroenterology, reproductive health, cardiology, and more:
We offer end-to-end document preparation, including study concept development, synopsis creation, full protocol drafting, investigator brochures, informed consent forms, and clinical trial reports. Additionally, we prepare articles for peer-reviewed journals based on study results, ensuring high-quality dissemination of findings.
Our team of experts provides comprehensive support in preparing and submitting documents to regulatory authorities and ethics committees.
We specialize in developing custom electronic case report forms (eCRFs) on Russian platforms and delivering detailed data analysis.
The charts below illustrate our extensive experience in conducting clinical trials across various therapeutic areas.
K-Research specializes in both international and local studies aimed at registering drugs within the Eurasian Economic Union (the Russian Federation, Armenia, Belarus, Kazakhstan).
Our team is composed of highly qualified professionals with years of experience in clinical research, ensuring exceptional service at every stage.
We craft personalized solutions to meet the unique needs and goals of each client, providing a truly customized experience.
We adhere strictly to international standards and regulatory requirements, delivering services of the highest quality with unwavering reliability.
By leveraging cutting-edge technologies and methodologies, we enhance the efficiency and accuracy of every study we conduct.
If you have any questions or would like to learn more about our services, feel free to reach out to us via phone or email. We would be delighted to discuss how we can assist you in achieving your clinical research goals.