ICON plc | Clinical Research Organisation (CRO) for Drug Development

Risk Based Quality Management

Essential for a robust monitoring strategy.

The evolution of HIV treatments

From antiretroviral therapy to vaccines, where we are today and what’s next.

ICER’s impact on payer decision making

Results of ICON’s third annual survey.

The IVDR journey

A roadmap to meet 2022 deadlines, while navigating pandemic disruptions.

Webinars

Upcoming webinar: Using wearables data to support drug reimbursement

18 May, 2021. Register now.

Long term effects of the COVID-19 pandemic on cardiovascular trial design

Upcoming webinar: Cardiovascular event adjudication during COVID-19 and beyond

21 May, 2021. Register now.

On-demand webinars

Visit our webinar channel to access other recent webinars.

Featured Services

COVID-19 clinical operations

Keeping your clinical trial on track in an evolving environment.

Site & Patient Solutions

Transforming recruitment through patient-centric trials and real-world, real-time data.

Biotech

ICON provides full service outsourcing and flexible support for biotech specific needs such as due diligence and asset valuation.

Functional Resourcing

From recruitment of a single clinical professional to managing entire global functions.

Biosimilars

ICON can support product design, development and registration, regulatory support and commercialisation of Biosimilars.

Increasing Site and Patient Compliance

FIRECREST: Digital solutions to increase efficiency in clinical trials by driving site performance.

ICON Insights

14 May 2021

10 lessons learned about secondary “real world” data strategy

Insights and lessons learned about operationalizing the use of real world data.

10 May 2021

Managed access programs as an alternative to long-term follow up studies

Managed Access Programs (MAPs), are one solution for early access to investigational products that are gaining traction.

06 May 2021

New procedures for drug prices negotiations and reimbursement in Italy

In March 2021 the Italian Medicines Agency adopted new guidelines for drug pricing and reimbursement decisions.

26 April 2021

The data revolution: Big data’s role in clinical trial patient recruitment, retention and engagement

How big data can be leveraged by pharma to solve key challenges in patient recruitment and drug development.

21 April 2021

The role of technology in Parkinson’s treatment and research

Constant study and innovation of Parkinson's Disease (PD) research has shown the implementation of medical devices, AI, and mobile applications pave the way forward.

20 April 2021

Event report - DIA Europe 2021: Advancing health priorities

Shradha Galaya, Director of Global Safety Regulatory Reporting, reports on the highlights of her recent virtual attendance at DIA Europe 2021.

14 April 2021

Biomarker assays: Bioanalytical meets CLIA

The blog considers current perspectives on the use of biomarkers, differences between the needs of biomarker assays developed for use in bioanalytical labs or clinical labs, and what may be needed in the case that a biomarker assay needs to migrate into a CLIA lab.

08 April 2021

Looking back and looking ahead: Trends in HEOR

In-person research became impossible due to the pandemic, and forced us to re-examine how patient's voices were being captured. In 2021 we continue to build on what we learned.

06 April 2021

Navigating complexity of cell therapy manufacturing during the COVID-19 pandemic

Over the past year, the COVID-19 pandemic significantly disrupted clinical research across the lifecycle including recruitment challenges, protocol amendments and delayed market entry.

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About ICON

ICON to acquire PRA Health Sciences

Clinical Study Match

The voice of NASH investigators

Antimicrobial resistance