Regulatory Affairs

Regulatory Compliance: CARU specializes in navigating the regulatory landscape of Central America, ensuring compliance with local regulations and international standards for clinical research.

Documentation Support: We provide comprehensive documentation support, assisting clients in preparing and submitting regulatory documents required for clinical trial approval in Central American countries. This includes managing the submissions of protocols and other necessary documents optimizing timelines and minimizing regulatory hurdles to expedite approval processes.

Ongoing Compliance Monitoring: CARU conducts ongoing compliance monitoring throughout the duration of the trial, ensuring that all regulatory requirements are met and maintained. We handle all submissions and regulatory interactions on behalf of our clients, providing a seamless and efficient regulatory affairs service.