For Sponsors and CROs
SMO Medical Technologies helps Sponsors and CROs reduce clinical trial operational risks: assess protocol feasibility, select Research Sites, start up the study, organize patient recruitment and enrollment, and control delivery quality.
We become involved at the feasibility stage and remain an operational partner through study completion.
For a Sponsor, the main risk in a clinical trial is losing time. Unrealistic recruitment estimates, slow Research Site activation and insufficient execution control can shift the timeline of the entire project.
For CROs, SMO Medical Technologies becomes one point of operational accountability across the Research Site network. This reduces the workload for the project team and simplifies communication.
Our services
Feasibility assessment
We analyze the protocol, inclusion and exclusion criteria, patient population, Research Site experience, infrastructure and potential enrollment timelines.
Study start-up and Research Site activation
We prepare Research Sites for study start: documentation, Investigator Site File, team training, scheduling and internal processes.
Patient recruitment, enrollment and screening
We use patient databases, referral chains, pre-screening and patient routing.
Research Site management
We coordinate timelines, documentation, visits, communication and compliance with unified standards.
Ethics committee and regulatory process support
We support document preparation, local approval processes and communication related to study start-up.
Monitoring support
We prepare Research Sites for monitor visits, coordinate schedules and review key documentation.
Research Site staff training
We provide training on the protocol, GCP, internal procedures and documentation requirements.
Need to assess protocol feasibility?
Send us the therapeutic area, study phase and key protocol criteria. We will prepare a preliminary assessment of enrollment potential, suitable Research Sites and timelines.