Frequently Asked Questions

AXIOS Clinicals is a global Clinical Research Organization (CRO) providing end-to-end clinical trial and research support services.

We work with pharmaceutical companies, biotechnology firms, medical device companies, research institutions, and healthcare organizations.

We support clinical trials across all phases, from early-phase studies through late-phase and post-market programs.

Yes. We provide full-service CRO delivery, including study start-up, monitoring, data management, medical writing, and close-out.

Our FSP model provides experienced clinical professionals who integrate seamlessly into sponsor teams on a flexible, scalable basis.

We operate globally, with strong experience across established and emerging markets, including hard-to-reach regions.

We conduct protocol feasibility assessments, site identification, performance evaluation, and enrollment forecasting to support informed trial decisions.

We operate in alignment with global regulatory standards and apply robust quality management systems across all trial activities.

Yes. We offer medical oversight, pharmacovigilance, safety reporting, and DSMB support to protect patient safety.

We work closely with sites to develop recruitment strategies, improve engagement, and reduce patient dropout.

Our teams have experience across multiple therapeutic areas. Specific expertise can be aligned to each study’s requirements.

Yes. We collaborate closely with investigators and sites to support operations, training, and study performance.

We apply risk-based quality management, data validation processes, and continuous oversight throughout the study lifecycle.

Yes. Emerging markets are a core strength, supported by local expertise and global standards.

Yes. We provide CRAs, project managers, data managers, safety specialists, and other clinical professionals.

We maintain transparent, structured communication with regular updates, reports, and issue escalation processes.

Our combination of global reach, experienced teams, operational discipline, and site-centric approach sets us apart.

Yes. We provide audit support, inspection readiness, and validation services across GCP, GMP, GLP, and CSV.

Sponsors can contact us through our website to schedule a discovery call or request a proposal.

Yes. We support broader healthcare, wellness, and research outcomes programs beyond traditional clinical trials.