From identifying biomarkers to improving clinical trial efficiency.
3 March, 2021. Register now.
8 April, 2021. Register now.
13 April, 2021. Register now.
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Keeping your clinical trial on track in an evolving environment.
Transforming recruitment through patient-centric trials and real-world, real-time data.
ICON provides full service outsourcing and flexible support for biotech specific needs such as due diligence and asset valuation.
From recruitment of a single clinical professional to managing entire global functions.
ICON can support product design, development and registration, regulatory support and commercialisation of Biosimilars.
FIRECREST: Digital solutions to increase efficiency in clinical trials by driving site performance.
The new In Vitro Diagnostic Regulation (IVDR) aims to harmonise regulatory framework across the European Union (EU) to ensure the safety and performance of devices by placing greater responsibility on manufacturers to demonstrate that their products meet stringent requirements.