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As the largest site network in Europe - and the world’s leading oncology research network - Pratia operates 100+ sites across eight countries, including the U.S and Turkey. We cover 85% of all therapeutic areas and run up to 600+ active clinical trials annually. In line with our mission to expand access to innovative treatments, we are strategically growing our global presence to reach and support diverse patient populations worldwide.
Find your local Pratia website:
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USA
Clinical Research Sites
Site Service Provision
Pratia’s U.S. footprint combines community-based research access with advanced early-phase oncology capabilities. We enable inclusive enrollment strategies and bring research closer to where patients receive care, supporting both early-phase oncology and broader clinical development programs. This expanding presence strengthens transatlantic study delivery within a unified research environment.
This approach guarantees simplified site selection, faster start-up, easy study scale-up, access to a broader pool of patients and experts, as well as unified quality and standardized data format from diverse sites across the globe.
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Global project oversight is provided for any multi-country study, supporting you in all matters between sites and CROs or sponsors while expediting start-up and facilitating project delivery. We deliver on our commitments through milestone tracking embedded in our project plans from start to finish. Our Global Project Management team accelerates study start-up activities and issues regular progress reports for your convenience.
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We offer a centralized feasibility process that ensures fast turnaround on requests for information and Yes/No decisions, country and site selection, patient mixes, and fully costed proposals. Budgets are consolidated per study, broken down by country, and tailored to any type of project. All feasibility assessments include scientific input from our investigators, minimizing the risk of site dropout and ensuring smooth study execution.
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We offer a ONE contract solution for all clients. One contract, available either as a CTA or a work order under an existing MSA, is all that is needed—regardless of the volume of sites and vendors per project. Pratia’s full contract cascade internally is available and auditable on request for complete transparency. ONE budget per country, ONE schedule of work globally, ONE invoice each month. All within FMV parameters.
The synergy across all Pratia sites is powered by our state-of-the-art proprietary technology, Hyggio. The software’s features - including eSource, CTMS, remote monitoring, patient recruitment, and more - drive operational efficiencies across all our sites while delivering cost savings for our clients.
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Thanks to unified electronic medical documentation that complies with FDA and EMA requirements, our clients receive the highest quality data - the cornerstone of scientific credibility in any study – on time.
Unified CTMS, finance, and budget modules ensure transparency and operational efficiency, saving crucial time and enabling seamless communication and collaboration with our clients.
Remote Monitoring enables convenient, remote access to visit records for protocol verification via SDV and SDR across the world, delivering major time and cost savings for clients.
Hyggio’s patient-dedicated module offers a robust data warehouse to enhance patient communication and recruitment, maximizing patient access to innovative treatments and accelerating recruitment timelines for clients.
Our Global Site Network is built on shared values, harmonized processes, and centralized support
- all guided by thoughtful technology and united vision. By connecting sites worldwide with a patient-centered focus, we help create more inclusive access to research.
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Anna Titkova
International Operations Director at Pratia
Discover how our flexible approach can support your unique study needs.
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