CNR Research provides one-stop integrated services covering all stages of clinical trials, from researcher selection to product approval (NDA). From clinical trial planning, IND application, trial operation, data management and statistical analysis, to report writing, we conduct clinical trials systematically and efficiently based on our expertise and experience at every stage.
We support the stable and successful execution of even complex clinical trials. With CNR Research, you can effectively achieve optimal clinical results that meet both quality and regulatory requirements.

As Korea’s leading Full‑Service CRO, C&R goes beyond simple clinical trial agency to act as a true research partner to our clients. From pharmaceuticals to medical devices, medical doctors and clinical statisticians are closely involved throughout the entire process, from the early stages of clinical trials to their completion, providing scientific and strategic guidance and comprehensive solutions that cover the entire clinical trial cycle.

CNR Research offers differentiated clinical solutions based on its experience in successfully conducting challenging clinical trials involving contrast agents, botulinum toxin, biopharmaceuticals, medical devices, and other products with complex mechanisms and high regulatory barriers. Even in clinical trials requiring complex indications and stringent regulatory requirements, we provide reliable, high-quality services based on our medical expertise and precise statistical analysis capabilities.

• Protocol Design & Regulatory Strategy: Medical doctors and statistical experts participate in establishing plans based on scientific evidence, from the initial research design to regulatory strategy.
• Medical Writing & Data Management: Ensuring the precise quality of clinical document creation and data management that meets regulatory requirements.
• Clinical Operation: Efficient clinical operations for various indications and highly complex products.
• Biostatistics & Statistical Programming: Professional clinical statistical analysis and interpretation capabilities.
• Pharmacovigilance & Medical Affairs: Safety evaluation during and after clinical trials, and medical communication
• Quality Management: Regulatory compliance management throughout the entire clinical trial process by operating a quality system based on SOPs and standard procedures
• Medical Device: Customized CRO specializing in medical devices throughout the entire cycle, including exploratory clinical trials and confirmatory clinical trials for approval, as well as clinical trials after approval

CNR Research is investing heavily in human resource development to ensure the sustainable growth and development of the clinical trial industry. CNR Academy is an educational institution established by CNR Research to provide systematic clinical education services at a global level and contribute to strengthening the capabilities of clinical trial professionals.

The skilled clinical professionals trained through CNR Academy play an important role in raising the quality of the clinical industry in South Korea to a higher level. This goes beyond simply cultivating human resources; it is CNR Research's core social contribution to strengthening the competitiveness of the entire clinical ecosystem and increasing the success rate of future new drug development.

Based on its role and responsibility as a leading CRO, CNR Research will continue to pioneer a bright future for the clinical industry in South Korea through CNR Academy.

Representative training programs include introductory and advanced courses for clinical research associates (CRAs), such as the Fundamental Course, Basic Course, and Monitoring Practice, which include theory and practical training, as well as the Clinical Project Management course for managers.
In addition, we offer specialized training programs in various clinical fields, such as oncology clinical trials, medical writing, DM/STAT, quality assurance, and regulatory affairs.

As an MFDS-officially designated and trusted clinical trial education institution, CNR Academy provides reliable clinical education services at a global level through continuous quality control and thorough verification of all education programs in accordance with international standards based on ISO 9001 certification.

imtrial is a data integration platform developed by CNR Research to contribute to the growth of the clinical trial industry.
Since 2018, we have been conducting research on standardization and automation of the planning, design, implementation, and submission processes of clinical research. Experts in various fields, including data management, medical statistics, and IT development, have come together at the Clinical Platform Research Institute to devote their best efforts to building this platform.

The platform is evolving to provide standard APIs that enable not only pharmaceutical companies, hospitals, and CROs directly involved in clinical research but also companies with an interest in the industry to easily access its advanced technology and innovative ideas. By doing so, imtrial will serve as a foundation for the clinical trial industry and the technology industry to grow together.

imtrial is a digital platform that enables faster and more efficient clinical trials, providing MDR (Metadata Repository) services for storing standardized data and TDLM (Trial Data Lifecycle Management) services for generating and converting clinical trial data.

The MDR, which stores standardized data, enables data utilization and reuse, thereby reducing work time and increasing work efficiency.
TDLM utilizes the standardized data in the MDR to automatically generate eCRFs.
It also automatically generates SDTM packages (Dataset, Define.xml, aCRF, SDRG) to enable fast work.