Frontivia Global | Services
Services
Commercial Focus
Academic Depth
Frontivia Global understands commercial timelines, investor pressures and regulatory scrutiny and we deliver with precision. We combine 25+ years of experience and academic research with pace and accountability of commercial delivery, with bespoke services.
Clinical Research Services
Designed Around Your Study
Frontivia Global provides flexible CRO solutions that support clinical research from study design and start-up through to delivery, analysis and reporting.
Our multidisciplinary teams combine expertise in clinical operations, biometrics, quality assurance and regulatory strategy to help sponsors navigate complexity, maintain compliance and generate high-quality clinical evidence.
Whether you're looking for a full-service CRO partner, specialist functional expertise or additional resource to strengthen your existing team, we tailor our approach around your programme, timelines and objectives.
Choose the Delivery Model That Fits Your Study
Every clinical trial is different. That's why we offer flexible delivery models designed to meet the needs of biotech, pharmaceutical, academic and healthcare organisations.
Full-Service CRO Delivery
Partner with a single experienced CRO to manage and coordinate your clinical research programme from start to finish.
Our integrated teams provide joined-up expertise across clinical operations, biometrics, quality, regulatory support and study management, creating a seamless experience with clear accountability throughout the study lifecycle.
Benefits include:
- Single point of contact
- Integrated project oversight
- Streamlined communication
- Consistent quality management
- Greater visibility of study progress
Functional & Bespoke Services
Need support in specific areas of your study?
Our specialist teams can work alongside your internal resources, existing CRO partners or study vendors, providing expertise exactly where it is needed.
From standalone data management and biostatistics support to tailored combinations of monitoring, quality assurance, regulatory and operational services, we provide flexible solutions that scale with your programme.
Services Across the Study Lifecycle
Expert clinical research services, delivered individually or together as part of a tailored or full-service CRO model.
Model-Informed Drug Development
- Digital Twin Modelling
- Trial Design Support and Development
- Evidence Generation
- Patient Selection including Biomarker Led Stratification Strategy
Project Management and Clinical Operations Support
- Site Selection and Start Up
- End-to-End Study Oversight
- Vendor Management
- Risk Management
- Trial Governance
- Clinical Site Monitoring
Clinical Data Management
- Database Design and Build
- Electronic Data Capture (EDC)
- Data Quality Oversight
- Database Lock
- Submission Support
Biostatistics & Statistical Programming
- Study Design Support
- Sample Size Calculations
- Statistical Analysis Plans
- CDISC Standards
- Regulatory Submissions
Medical Writing & Regulatory Support
- Protocols
- Clinical Study Reports
- Regulatory Documentation
Let's move your research forward
Whether you're planning a new study, seeking specialist expertise or looking for a CRO partner to support an existing programme, we'd welcome the opportunity to discuss your requirements.
Complete the form below and a member of our team will be in touch.