Clinical Research IMPACT Organization
Our commitment is to accelerate clinical research and bring innovative therapies to market.
What is CRIO?
CRIO is an academic CRO that aims to bridge biomedical research with clinical practice, facilitating the integration of new technologies and advanced therapies to improve people’s health and quality of life. To achieve this, we have top-tier infrastructure and a strong focus on regulatory compliance. Additionally, we establish strategic partnerships to make the execution of early-stage clinical trials in scientific and technological development possible.
CRIO offers comprehensive clinical research services, from study design to the final report, focused on enabling high-quality clinical trials and validating the safety and efficacy of technologies with real clinical applications.
Mision
Vision
Our mission is to assist in the development of advanced clinical research through comprehensive and collaborative support for researchers and physicians, ensuring regulatory compliance, efficiency in study execution, and the transfer of knowledge to clinical practice to improve people’s health and accelerate access to accessible, high-quality therapeutic innovations.
We want to be an international leader in academic clinical research, recognized for accelerating the development and validation of advanced therapies that transform health and quality of life, by connecting science, technology, and clinical practice in an ethical and excellence-driven environment.
Why choose us?
CRIO is more than just a clinical services provider; it is a strategic partner in the research and development of advanced therapies. Our commitment is to make the most cutting-edge therapies accessible, affordable, and effective, helping researchers and companies overcome the challenges of clinical development within a regulated environment.
Excellence in academic research
Comprehensive support in clinical trials
Specialized infrastructure and resources
Focus on knowledge transfer and research
Leveraging the expertise of leading biomedical researchers and collaboration with prestigious institutions, CRIO provides an environment that combines academic rigor with clinical guidance. This facilitates the development of innovative therapies, meeting the highest scientific standards.
From protocol design to the implementation and analysis of clinical trials, CRIO provides end-to-end support, removing operational obstacles and enabling researchers to focus on scientific advancement. Our team ensures that every phase of the study is aligned with both international and national regulatory and ethical standards.
CRIO features advanced infrastructure, including access to biotechnology laboratories (cytometry, GLP laboratories), an animal facility, and GMP-grade advanced therapy manufacturing, ensuring the efficient development of complex technologies such as cell therapies, gene therapies, and artificial intelligence applied to healthcare.
We foster the transformation of academic research into viable clinical solutions. Our mission is to support technologies and therapies that can improve patient health, creating tangible value for both the medical community and the academic ecosystem.
Services
We prepare and submit all the necessary documentation for approvals from the Scientific Ethics Committee and health services reviews, as well as manage all required documentation for approval by the Public Health Institute (ISP) in Chile.
Our team specializes in clinical trial design, focusing on scientifically robust protocols that comply with national and international regulatory standards. From early-phase trials to more complex late-phase studies, CRIO ensures that every detail is meticulously planned.
This includes the development of customized proposals to meet the stringent requirements of the diverse public funding sources in Chile, ensuring the highest chances of success.
Once funding is secured, CRIO provides comprehensive financial management services, ensuring that funds are allocated and used efficiently throughout the entire project lifecycle.
CRIO expands the reach of clinical trials by identifying and opening new study centers, both locally and internationally, to ensure a broad and diverse patient group.
CRIO provides direct access to patient populations for clinical trials, ensuring timely and efficient recruitment at the Clínica Universidad de los Andes and other centers.
Our on-site monitoring teams ensure protocol compliance, patient safety, and data integrity throughout the clinical trial, providing real-time oversight and support.
CRIO offers advanced sample processing services at our Good Laboratory Practice (GLP) certified facilities, ensuring that all samples are handled with the highest standards of quality and precision.
Our experienced team of biostatistics and data analysis provides comprehensive analysis services, transforming raw data into actionable insights. We deliver a detailed and thorough final report, summarizing findings and providing recommendations for future research or commercial applications.
Our team
