Oslomed – Clinical Trial Site Organization
Reliable Site Performance for Your Clinical Trials
Sponsors and CROs partner with Oslomed to confidently deliver successful clinical trials for drugs, medical devices, diagnostics, and combination products in Central Europe.
Built for efficient, high-quality trial execution
Backed by extensive experience with Sponsors and CROs, Oslomed’s team is built to ensure quality, consistency, and operational efficiency in every clinical trial.
Integrated operations
Rapid feasibility responses and efficient contracting with dedicated support / project management
Accelerated study initiation
With complete site documentation and operational infrastructure in place, Oslomed’s experienced team is ready for immediate site initiation and accelerated patient enrollment
Strong patient networks
Targeted recruitment strategies and effective patient retention programs to achieve enrollment goals
Quality oversight & data integrity
Quality monitoring and management rigorously maintained through standardized procedures and documentation tools
Streamlined operation for efficient site engagement
Our team provides rapid feasibility responses and maintains transparent communication throughout your trial—from initial assessment through study completion.
Your team works with a single, dedicated contact who ensures consistent oversight, timely updates, and standardized processes across all study activities.
Our investigators can, if needed, provide their clinical expertise and practical experience as input to sponsors to support protocol optimization, realistic enrollment planning, and efficient trial execution.
Responsive feasibility and contracting
- Single point of contact for streamlined coordination
- Protocol-based enrollment projections using site data
Systematic approach to accelerate study start-up
At Oslomed, our experienced team and streamlined operational procedures ensure fast and efficient study activation. Investigators and coordinators are ready for immediate protocol training and site initiation visits.
Expedited Activation
Efficient, coordinated site activation that minimizes time from selection to readiness.
Pre-Established Infrastructure
Operating and well-equipped medical center with +8000 patients a year.
Pre-Qualified Vendors
Established contracts with laboratories, imaging centers, and pharmacies enable immediate site activation.
Strategic patient engagement for enrollment success
Oslomed applies targeted recruitment strategies to achieve enrollment objectives, including hard-to-reach populations and specialty indications.
Patient database
- • Early recruitment planning upon study initiation
- • Community engagement and diversity outreach
Targeted campaigns
- • Study-specific local recruitment efforts
- • Participant retention and adherence support
Specialty access
- • Defined therapeutic populations
- • Specialized procedures and equipment
Comprehensive quality management and data accuracy
Oslomed ensures research quality through a structured SOP system. Site personnel provide ongoing oversight of data quality and protocol adherence, with access to consultations from QA specialists.
Rapid Data Management
Efficient data entry and query resolution processes
Quality Management
SOP-driven processes with continuous oversight for quality and compliance
Discuss your research program with Oslomed
Contact our clinical trials team to explore how we can support your upcoming studies
Location
Kraków, Poland