Who We Are
ASSAY started off in 2012 with a group of seasoned clinical research professionals providing project management and clinical trial management services.
We are a technology-driven CRO, focusing on developing innovative software solutions for running clinical trials. With an agile engineering and IT division collaborating alongside clinical scientists in India and the UK, ASSAY builds robust, customized solutions based on study needs to increase trial efficiency, data integrity, and compliance.
Patient Safety & Data Quality
Patient safety and high-fidelity data are of paramount importance for ASSAY. We achieve this by deploying specialized clinical talent and proprietary e-clinical technologies, ensuring our collective expertise maximizes trial success and accelerates time-to-market.
Pioneering the Futuristic CRO
ASSAY aims to be the global benchmark in harmonizing trial management with breakthrough digital systems. We are committed to leading the paradigm shift as a tech-enabled, agile CRO that simplifies complexity for sponsors worldwide.
Global Reach & Therapeutic Strengths
ASSAY has established a trusted presence in both established and high-recruitment emerging territories. With our headquarters in the UK, we oversee European studies. Our operational hubs in India extend across Asia—including Sri Lanka, Bangladesh, Singapore, Thailand, and Malaysia. In addition, we support high-impact studies across West Africa and Sub-Saharan regions (including Sierra Leone).
Our strategic positioning makes us the preferred partner for challenging therapeutic domains:
Our Commitment to Quality
At ASSAY, we dedicate substantial effort toward proactive risk management. In high-risk territories, ASSAY by default includes additional site and CRA quality assessment visits to ensure root causes are addressed immediately and a robust CAPA is maintained.
Our quality assurance framework guarantees compliance with ICH-GCP, FDA 21 CFR Part 11, EMA, and MHRA regulations.
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