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ICON plc
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    Our services span the entire lifecycle of product development and commercialisation, and can be adapted to suit small local trials or large global programs.

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    Bringing the clinical trial to the patient with innovation and in-home solutions.

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    ICON provides its full range of clinical, consulting and commercial services across several industry sectors.

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

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

    Serving governments, multinational public health organisations, and global NGOs.
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    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.

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    CardiovascularCell and Gene TherapiesCentral Nervous SystemEndocrine & Metabolic DisordersInfectious DiseasesInternal Medicine & ImmunologyMedical DeviceOncologyRare & Orphan DiseasesTransplant ImmunologyWomen's Health
    ICON has recently led the development of 17 vaccines resulting in FDA/EMA approvals. We are currently working on a number of COVID-19 vaccine trials.
    Vaccines

    ICON has recently led the development of 17 vaccines resulting in FDA/EMA approvals. We are currently working on a number of COVID-19 vaccine trials.

    ICON's therapeutic experts contribute regularly to industry publications and the creation of thought leadership content. Read more.
    Therapeutics insights

    ICON's therapeutic experts contribute regularly to industry publications and the creation of thought leadership content. Read more.

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    We develop integrated technologies to significantly enhance the efficiency and productivity of clients’ drug and device development programs.

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    With travel restrictions due to COVID-19, FIRECREST helps deliver and manage remote training for investigators.
    FIRECREST

    With travel restrictions due to COVID-19, FIRECREST helps deliver and manage remote training for investigators.

    Connecting patients with the right trial in the right location.
    Patient Engagement Platform

    Connecting patients with the right trial in the right location.

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    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.

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    Decentralised & hybrid clinical trials

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    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.

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    ICON to acquire PRA Health Sciences

    Creating a world leader in healthcare intelligence and clinical research.

    3 March, 2021
    Webinar: HIV treatments from antiretroviral therapy to vaccines

    3 March, 2021

  • About ICON

    About ICON

    Our mission is to help clients accelerate the development of drugs and devices that save lives and improve quality of life.

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    About ICON
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    ICON is committed to making a positive impact on our people, environment and our community.
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  4. Patient Engagement Web Platform from ICON Bolsters Clinical Connectivity

Patient Engagement Web Platform from ICON Bolsters Clinical Connectivity

  • 13 May 2019

An Outsourcing Pharma article featuring commentary from experts EB McLindon & Gretchen Goller, on ICON’s new web-based patient engagement platform to provide patients with study-specific information and connectivity.

View Article

Related Information

Media Article

Patient engagement web platform from Icon bolsters clinical connectivity

Webpage

Patient Engagement Platform

Webinar

From Big Data to Patient Engagement in Clinical Trials

Press Release

ICON Launches New Patient Engagement Platform to Support Improved Patient Experience and Enrolment in Clinical Trials

Webpage

Late Phase Patient and Site Engagement

Webinar

Engagement and Retention of Patients in Rare/Orphan Disease Clinical Trials

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