Our services span the entire lifecycle of product
development and commercialisation, and can be adapted to
suit small local trials or large global programs.
Keeping your clinical trial on track in an evolving environment.
Site and patient identification, enrolment and engagement.
ICON provides its full range of clinical, consulting and commercial services across several industry sectors.
The new EU medical and in vitro diagnostic device regulations go into effect at the start of 2020. Are you ready?
Serving governments, multinational public health organisations, and global NGOs
We have extensive experience in a broad range of therapeutic areas. Managing studies in all major geographies, we have established solid working relationships with the world’s leading investigators.
ICON has conducted hundreds of clinical studies in both solid and haematological tumours, including experience with CAR-T therapies.
ICON has recently led the development of 17 vaccines resulting in FDA/EMA approvals.
We develop integrated technologies to significantly enhance the efficiency and productivity of clients’ drug and device development programs.
Using data to design, simulate, and analyse adaptive clinical trials with ease.
Connecting patients with the right trial in the right location.
BioPharma companies and Medical Devices manufacturers face growing operational, regulatory and economic challenges. ICON provides analysis and key insights on these challenges, with practical advice and recommendations.
Real time statistics, news and social media updates.
Reduce post market study costs with Real World Data.
ICON regularly contributes thought leadership to industry media publications and conferences, and has been recognised as one of the world’s leading Contract Research Organisations through a number of high-profile industry awards.
Access a wide range of on-demand webinars
The challenges and opportunities for rare disease drug development
Our mission is to help clients accelerate the development of
drugs and devices that save lives and improve quality of life.
We are committed to exceeding the quality standards demanded by our clients, patients and regulatory authorities.
Partners Making a Difference.
Download our case study to discover ICON’s operational expertise, proven execution processes & technologies that maintain study blinding & prevent operational bias in adaptive design trials -- increasing clients' chances of success
After running for seven years, an adaptive Phase II trial for acute infectious diarrhea fell prey to operational bias during interim analysis. Learn which procedures could have enabled the study to maintain blinding.
Learn how ICON’s operational expertise, proven execution processes, and technologies maintain study blinding and prevent operational bias in adaptive design trials. Download your copy today.