Accelerating Clinical Trials Through Precision & Innovation
Assay Clinical Research partners with global pharmaceutical, biotechnology, and medical device sponsors to deliver audit-ready, data-driven, and highly compliant Phase I–IV clinical development programs.
Dedicated to Clinical Excellence Since 2012
ASSAY Clinical Research was founded in 2012 by a seasoned group of clinical research professionals. Headquartered in the United Kingdom, our reach extends across the UK, Europe, Asia, and West Africa.
We deliver tailored clinical trial management solutions based on emerging technologies and robust scientific methodologies. Whether you are a multinational pharmaceutical sponsor, an emerging biotech, or a medical device innovator, our dedicated teams stand ready to guide your protocol to success.
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Full-Spectrum Clinical Development Services
We tailor our operational frameworks to meet the exact complexity of your study protocol and therapeutic domain.
Clinical Trial Management
Comprehensive oversight of clinical trials from protocol feasibility and ethics submissions to monitoring, data collection, and clinical study reports.
Explore Trial ManagementProprietary Clinical Technology
Cloud-native CTMS, integrated e-TMF, and electronic investigator site files (e-ISF) that streamline collaboration, reduce trial overhead, and ensure audit readiness.
Explore Tech SuiteStrategic Resourcing & Staffing
Access high-caliber, GCP-trained Clinical Research Associates (CRAs), Project Managers, and Medical Monitors on flexible dedicated or functional service models.
View Resourcing ModelsPhase I–IV Studies Delivery
Expertise spanning early first-in-human Phase I pharmacokinetics to large-scale international Phase III confirmatory trials and post-marketing surveillance.
View Phase CapabilitiesGRAVITY & EFES Platforms
Our dedicated platforms for clinical feasibility scoring, electronic investigator portals, and real-time trial progress dashboards accessible anywhere in the world.
Discover GRAVITYRegulatory & Quality Assurance
Expert advisory for protocol design, ethics committee applications, independent site auditing, and comprehensive inspection readiness.
Consult Quality ExpertsBuilt for Transparency, Compliance & Speed
Modern clinical trials require intuitive digital tools that eliminate redundant paper trails and accelerate data visibility. AssayCR has engineered a connected technology ecosystem to guarantee seamless collaboration.
GRAVITY Clinical Management System
Centralized milestone tracking, site payment triggers, document repositories, and investigator contact matrices.
EFES Feasibility Engine
Intelligent algorithm-driven investigator site selection, patient recruitment forecasting, and regional timeline estimation.
Integrated e-TMF & e-ISF Synchronization
Live document verification following DIA TMF Reference Model standards with instant sponsor audit access.
AssayCR Clinical Cloud
Enterprise Security | 256-bit EncryptionInterested in a live interactive demonstration for your clinical team?
Request Platform DemoExplore Our Publications & Digital Brochures
Read our interactive flipbooks and technical white papers regarding trial management, regional capabilities, and innovation.
Assay Corporate Overview
Discover our core philosophy, organizational structure, and clinical trial delivery standards.
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GRAVITY Platform Guide
Comprehensive technical specification of our trial management system and document modules.
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vShare Technology
Next-gen investigator file sharing and secure communication architecture for research sites.
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West Africa Operations
Joint training initiatives and emerging market trial execution in high-recruitment territories.
Read Digital FlipbookWhat Industry Leaders Say About AssayCR
Trusted by global pharmaceutical sponsors and international CRO partners to rescue complex protocols and deliver timely outcomes.
"In the present-day industry, finding the right candidate for a complex protocol is increasingly demanding. Need for a robust candidate database and precise communication skills are key. ASSAY provided us with exceptional talent on time."
"We were experiencing paper CRF challenges for a rare disease study closed post-audit. ASSAY and its team of seasoned CRAs completed the extensive monitoring, SDV, and retrieval well ahead of critical regulatory deadlines."
"We approached ASSAY for monitoring services for a Phase I Oncology trial. Owing to the challenging nature of the study, we required exclusive attention and rigorous quality. ASSAY delivered beyond expectations, making them our ongoing partner."
Ready to Accelerate Your Clinical Protocol?
Get in touch with our clinical research and regulatory specialists to evaluate site feasibility, resourcing timelines, and budget estimation.