Global Clinical Development Built Around Biotech Innovation
Global clinical development is about more than opening sites in multiple countries. Multinational programs require consistent program governance, integrated Clinical Operations, coordinated Regulatory Affairs, experienced regional teams and one accountable partner.
Evestia Clinical combines central program leadership with local operational expertise. Our Full-Service CRO and FSP Solutions models provide flexible, agile program delivery, working as an integrated scientific partner throughout global clinical development.
One Accountable Partner
Central program governance across every participating country, with a single point of accountability for operational quality and timelines.
Local Expertise, Global Oversight
Regional regulatory knowledge and established investigator relationships, coordinated through central program leadership.
Senior Engagement Throughout
Senior leaders who remain directly engaged throughout international program delivery. Faster decisions, greater program continuity at every milestone.
Flexible Delivery Models
Full-Service CRO and FSP Solutions that scale with program complexity and program evolution, without permanent infrastructure investment.
Built for Global Clinical Development
Successful multinational development depends on more than geographical reach. It requires one accountable partner, integrated scientific leadership, regional operational expertise and consistent program governance coordinated across every participating country.
Evestia Clinical provides centralized program leadership alongside regional regulatory and operational knowledge, maintaining coordinated regulatory strategy and multinational program continuity from study initiation through global submission. Sponsors work with one team, one governance model and one committed partner throughout every stage of international development.
Global Reach at a Glance
With 12 offices across 10 countries spanning Europe, North America and Asia-Pacific, Evestia Clinical combines global program leadership with local expertise to support successful multinational studies.
12+
Offices Worldwide
Across 10 countries
Europe, NA & APAC
Regional Coverage
Three major clinical markets
Phase I–IV & Post Marketing
Clinical Development Support
End-to-end global delivery
Global
Regulatory & Operational Expertise
FDA, EMA, MHRA and beyond
Global Clinical Development Network
Hover over each region to explore our clinical development capabilities, regulatory expertise and operational presence across global markets.
12
Offices
3
Regions
24/7
Global Support
Why Global Reach Matters
Successful clinical development is built upon access to international patient populations, specialist investigator sites and region-specific regulatory expertise.
Evestia Clinical combines global program oversight with local operational knowledge to help sponsors coordinate multinational clinical programs. Our Clinical Operations and Regulatory Affairs teams coordinate across jurisdictions, from study planning through final submission.
- Support efficient international patient recruitment through established site networks
- Access specialist treatment centers across multiple countries
- Coordinate regional regulatory requirements across FDA, EMA and MHRA
- Maintain consistent study quality across global investigator sites
- Support multinational Phase I–IV & Post-Marketing programs from a single accountable partner
Global Quality Standards
All Evestia Clinical programs are delivered under harmonised quality systems aligned with ICH-GCP, regional regulatory requirements and sponsor-specific governance expectations.
Our integrated quality framework helps ensure consistency, compliance and coordinated operational delivery across multinational clinical development programs, from Phase I first-in-human studies through global Phase III registration studies.
ICH-GCP Aligned
All programs delivered under harmonised quality systems meeting international GCP standards.
Multi-Jurisdictional
Regulatory expertise across FDA, EMA, MHRA and additional global health authorities.
Centralized Oversight
Integrated governance ensuring consistent quality and operational standards across all sites.
Experienced Teams
Senior clinical professionals with direct experience across multinational program delivery.
Regional Clinical Development Expertise
Operational teams with regional knowledge, regulatory familiarity and established investigator networks across Europe, North America and Asia-Pacific.
Europe
Supporting studies across major European clinical research markets from offices in Letchworth Garden City, Berlin, Lyon, Madrid, Milan, Warsaw, Steinhausen and Hoofddorp.
Regional Capabilities
Countries
United Kingdom, Germany, France, Spain, Italy, Poland, Switzerland, Netherlands
Office Locations
North America
Supporting clinical development programs through US-based operational expertise across offices in Charlottesville, Boston and South San Francisco, combined with global program leadership and sponsor engagement.
Regional Capabilities
Countries
United States
Office Locations
Asia-Pacific
Providing regional support for international clinical development programs and global study execution across Asia-Pacific markets from our office in Iluka, Western Australia.
Regional Capabilities
Countries
Australia
Office Locations
Global Regulatory Expertise
International clinical trials require coordinated regulatory submissions, ethics approvals and country-specific requirements across multiple jurisdictions simultaneously.
Integrated Regulatory Affairs expertise streamlines submissions and supports coordinated program delivery. Our regulatory teams have experience across:
Integrated regulatory strategy from Study Start-Up through submission supports coordinated program delivery across multinational clinical development programs.
Access to Specialist Patient Populations
Many programs require access to geographically dispersed patient populations and specialist treatment centers, particularly where populations are small or concentrated at specialist sites.
Our global infrastructure provides access to specialist investigators, treatment centers and patient populations, supporting patient-centerd recruitment strategies and sustained program enrollment.
Oncology CRO
Access to specialist oncology centers and investigator networks globally.
Rare Disease CRO
Reaching dispersed patient populations for ultra-rare conditions.
Neurology CRO
Specialist neurology and neurodegenerative disease investigator sites.
Cell & Gene Therapy CRO
Advanced therapy treatment centers across key global markets.
Global Program Delivery Beyond Office Locations
While Evestia Clinical maintains offices across key clinical research markets, our operational reach is strengthened through established investigator networks, strategic partnerships and coordinated study management.
Our Clinical Trial Management teams coordinate multinational program delivery through centralized governance and oversight that spans geographies and regulatory environments. As a Global CRO, we support sponsors preparing for international studies or extending existing programs into new markets.
Supporting Global Programs Across Every Phase
Global CRO
Specialist international clinical development services for multinational programs.
Clinical Operations
Central oversight and coordination across global development programs.
Clinical Trial Management
Strategic leadership for complex international studies.
Regulatory Affairs
Multi-jurisdictional regulatory strategy and submission support.
Phase I CRO
First-in-human and early-phase studies across global sites.
Phase II CRO
Proof-of-concept and dose-optimization programs internationally.
Phase III CRO
Multinational registration studies and global regulatory approval.
Why Sponsors Choose Evestia Clinical for Global Development
One Accountable Global Partner
Central program leadership with coordinated regional delivery across every participating country.
Regional Expertise
Experienced teams with local regulatory and operational knowledge across Europe, North America and Asia-Pacific.
Flexible Delivery Models
Full-Service CRO and Functional Service Provider support tailored to sponsor needs and program evolution.
Built for Biotechnology
Supporting growing biotechnology organizations through flexible resourcing, scientific collaboration and senior program leadership.
Ready to Discuss Your Global Development Program?
Whether expanding into international markets or managing a multinational registration program, Evestia Clinical provides integrated delivery, regional expertise and global infrastructure to advance your development program.
Our teams combine regional knowledge with centralized oversight across Phase I through Phase IV & Post-Marketing, spanning Oncology, Rare Disease and other specialist therapeutic areas.