Are you searching for a reliable, experienced, and results-driven Clinical Research Organization (CRO) in Mexico? Look no further than Althian, a leading provider of comprehensive clinical research services in Latin America.
With over 17 years of experience conducting clinical trials in Mexico, we specialize in supporting pharmaceutical companies, biotechnology firms, and medical device manufacturers worldwide.
Our mission is to accelerate the development of innovative therapies while ensuring the highest standards of quality, compliance, and patient safety.
As a trusted and experienced Clinical Research Organization (CRO) in Mexico, Althian partners with pharmaceutical companies, biotech firms, and medical device manufacturers to deliver high-quality clinical trials in Mexico and Latin America. We specialize in providing end-to-end clinical research solutions, helping sponsors with or without a local presence navigate every step of the process seamlessly.
With deep expertise in COFEPRIS clinical trial regulations, ICH-GCP standards, and international compliance requirements (FDA, EMA), we ensure your study meets the highest levels of quality, accuracy, and patient safety.
Our multidisciplinary team manages the entire research lifecycle, from protocol development and site selection to patient recruitment in Mexico, logistics, and regulatory submissions.
From study design to execution
Ensuring ethical & legal standards
By combining local CRO expertise in Mexico with global best practices, Althian accelerates the success of clinical trials in Latin America, reduces risks, and delivers validated data that supports faster market entry for innovative treatments.
Partner with Althian – your gateway to successful, compliant, and efficient clinical research in Mexico.
Partner with Althian – your gateway to successful, compliant, and efficient clinical research in Mexico.
At Althian, we understand the importance of conducting clinical trials in compliance with regulatory requirements and industry best practices.
Comprehensive support for the design, implementation, and management of clinical trials, ensuring they are conducted efficiently and comply with all regulatory requirements.
Handling of all regulatory aspects of clinical trials, including submissions, compliance with local and international regulations, and communication with regulatory bodies.
Collection, processing, and analysis of clinical trial data to ensure accuracy, integrity, and reliability of results.
Continuous monitoring and evaluation of the safety profile of drugs, including detection, assessment, understanding, and prevention of adverse effects or other drug-related problems.
At Althian Clinical Research, we specialize in delivering comprehensive clinical research services from start to finish. Our expertise covers a broad spectrum of clinical studies, focusing on phase II to phase IV trials, including bioavailability and bioequivalence studies across Mexico.
