Since 2009, SMO Medical Technologies has built 15+ years of specialized expertise as a Site Management Organization in clinical trials.
The company manages its own research site network and brings years of proven, hands-on experience in patient recruitment, research site management, quality control, and clinical trial operations.
We act as an operational partner for Sponsors, CROs and Research Sites by combining medical expertise, patient access, process management and data quality within one system.
Company profile
SMO Medical Technologies manages Research Sites conducting Phase I–IV clinical trials, bioequivalence studies, pharmacokinetic and pharmacodynamic studies, post-marketing studies and specialized protocols.
Our work begins before study start. We analyze the protocol, assess the available patient population, select suitable Research Sites, prepare teams and documentation, organize screening and support the study through completion.
The core value of SMO Medical Technologies is manageability. Sponsors and CROs receive a single operational network with clear accountability, transparent communication, and unified working standards — not a scattered set of disconnected sites.
How we work
Feasibility and Research Site selection
We assess the protocol, patient population, infrastructure and Research Site capabilities.
Study start-up
We prepare documentation, teams, schedules, Investigator Site File and Research Site processes.
Enrollment and visits
We organize screening, patient routing, visits and patient retention in protocol.
Monitoring and quality
We support monitoring readiness, documentation control, deviation management and CAPA.
Research Site network
SMO Medical Technologies brings together private and public Research Sites with different therapeutic profiles, study phases and formats of care: inpatient care, day care and outpatient visits.
View Research SitesQuality and inspection readiness
For SMO Medical Technologies, quality is not a final check before an audit. It is a continuous working system.
This approach reduces the risk of delays, repeated queries, protocol deviations and open findings after audits.
Team
The SMO Medical Technologies team brings together investigators, study coordinators, quality specialists, nurses, documentation specialists and operational managers.
We see a clinical trial not only as a medical process, but also as a complex operational system where timelines, communication, data accuracy, patient routing and team readiness for every visit are critical.
Technology and data transparency
For international Sponsors and CROs, it is important to see ongoing study status: activation progress, enrollment pace, documentation readiness, risks and deviations.
Discuss your study with the SMO Medical Technologies team
Tell us about your protocol, therapeutic area and expected timelines. We will assess recruitment potential, suitable Research Sites and the possible operational pathway for the study.