Pratia Research Site Network offers two key service lines, ensuring a safe environment for all clinical trial stakeholders - patients, sponsors, and investigators - whilst delivering high-quality, compliant trial execution across all operational models.
Operational Capabilities & Expertise
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Lines of Service
End-to-end site operations
Pratia provides full operational leadership at the site level, taking clear ownership and responsibility for study delivery from start-up through close-out. We deliver comprehensive clinical trial execution at the site level, managing every step from study start-up to close-out across a wide range of therapeutic areas at our own dedicated research sites and embedded units. Whether for early-phase research, or larger-scale phase II-IV and decentralized trials, Pratia provides end-to-end solutions covering:
Feasibility & Study Start-Up:
Comprehensive site assessments, contracting and staff training to ensure an efficient trial launch.
Patient Recruitment & Retention:
Access to a broad patient base with strong informed consent and retention strategies to ensure patient satisfaction and study success.
Trial Conduct & Data Collection:
Protocol-based clinical study conduct, including patient reimbursement, secure IP management, and real-time data entry, to maintain accuracy and compliance.
Study Close-Out & Compliance:
Final patient visits, data verification, regulatory documentation, and audit readiness.
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Depending on trial requirements, we also provide expertise and capabilities in:
Clinical and non-clinical trial strategy consulting
Medical writing: protocol, ICF, CRF
Pharmacokinetics & Biostatistics
Biosampling
Site Service Provision (SSP)
Supporting your study with expert staffing while you retain full operational oversight. Site Service Provision (SSP) is the model we use to deploy highly qualified Study Coordinators and other specialized clinical research professionals to support multicenter studies across a wide range of therapeutic areas. With more than 20 years of experience delivering this approach, Pratia strengthens site performance while ensuring consistency, flexibility, and efficiency throughout study execution. Backed by advanced in-house technology, we provide real-time monitoring, customized reporting, and KPI tracking, ensuring flexibility, transparency, and optimized performance at every site. Our SSP covers:
Supply of Data Entry Specialists, Study Coordinators, and Nurses
Site identification and feasibility assessments
Quality control and compliance oversight
Clinical Trial Agreement (CTA) management
Why choose Pratia’s SSP offer?
Trust is the foundation of every successful partnership.
Our strength lies in understanding our clients’ challenges and working collaboratively to deliver tailored solutions that accelerate clinical development.
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Chloe Rose
Executive Director Portfolio Management
Ready to start your clinical trial?
Discover how our flexible approach can support your unique study needs.