EXCELLENCE IN CLINICAL TRIALS
A New Standard in Clinical Development, Small Enough to Care Big Enough to Deliver
Frontivia Global combines 25 + years of clinical trial development with the scientific depth of an internationally respected clinical research organisation with the agile, accountability and responsive approach required by pharma, biotech, diagnostic and academic sponsors. Small enough to care. Big enough to deliver.
Our multidisciplinary teams bring expertise across site start-up, project management and clinical delivery, biometrics, quality assurance and regulatory strategy, helping sponsors generate robust evidence, meet regulatory requirements and progress clinical development.
Delivering for Pharma,
Biotech, Diagnostic & Academia
With more than 25+ years of global clinical research experience, from peri-IND to commercialisation, Frontivia Global partners with you to accelerate your clinical development programme, with a tailored approach underpinned by robust data, evidence, and advice from leading clinical and scientific experts.
We combine scientific and operational expertise with an agile, accountable and responsive approach. Our teams work closely with sponsors, investigators, clinical sites and research networks to deliver accurate, compliant data and evidence throughout the clinical trial lifecycle. Our partnership with a Phase I unit offers opportunities for healthy volunteer and patient population studies.
It’s never too early to have a line of sight all the way through to market access. Frontivia Global provides services from a single specialist service to global clinical trial delivery, talk to us about what your study needs.
Built for Success
Frontivia Global combines 25+ years of experience and worldwide academic research with the same rigour, pace and accountability of commercial delivery. We understand timelines, investor pressures and regulatory scrutiny - and we deliver with precision and passion with commercial focus, scientific excellence, patient focus and academic depth
Clinical Development Services
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
Patient-Centred.
Outcome-Focused.
Participants are at the heart of every successful trial. Our tailored engagement strategies enhance recruitment, strengthen retention, and improve the patient experience, helping sponsors reach critical milestones faster.
Therapeutic Expertise.
In Depth Pre Clinical and Clinical Research and Development Experience and Expertise in Multiple Therapeutic Areas
Frontivia Global has experience across oncology, woman’s health, rare disease, neurology, mental health, pain and respiratory research, and beyond. This is underpinned by strong clinical trial methodology, operational and biometrics expertise that can be applied across different therapeutic areas and study designs.
Oncology
Extensive experience supporting complex international oncology trials across cancer types, treatment settings and all stages of clinical research.
Pain
Experienced support for pain studies, including complex patient populations, subjective endpoints and the challenges of measuring individual treatment response.
Neurology
Specialist clinical research support for neurological conditions, combining robust study design, data management, analysis and meaningful outcome measurement.
Respiratory
Collaborative clinical research expertise supporting well-designed respiratory studies, consistent data collection, robust endpoints and high-quality trial delivery.
Women's Health
Dedicated expertise in women’s health trials, from gynaecological and breast cancers to endometriosis and menopause, with study designs built around the input and needs of women across every stage of clinical research.
Rare Disease
Proven experience delivering rare disease trials across small and geographically dispersed patient populations, with flexible designs, global site networks and data expertise built for studies where every patient counts.
Mental Health
Thoughtful, rigorous clinical research support with expertise in patient-reported outcomes, assessment tools, data quality and statistical methodology.
Built on Experience
Focused on Delivery
Why Frontivia?
Clinical research is complex. Working with your CRO shouldn’t be. We combine scientific expertise with a practical, collaborative approach to deliver high-quality research.
Years of Trial Development
Patients Reached
Peer Reviewed Publications
Centres*
Countries*
Patients Screened*
*across a major international oncology study
Let's Work Together
At Frontivia Global, we strive to enhance your clinical development experience by providing timely and effective value-added solutions. We encourage you to complete the form below so we can respond to your queries about our services with utmost professionalism and care.