In the News
ICON experts frequently author or contribute to industry trade press.
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Embracing Biosimilars
Ioannis Katsoulis, Axel Svedbom, Larushka Mellor and rjan kerborg consider trends and strategies to drive uptake of biosimilars in the UK.
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The path to successful HTA submissions
For companies launching their products globally, gaining market access and reimbursement through HTA reviews is extremely challenging due to these nuances. Manpreet Sidhu discusses the factors that are key to success in achieving favourable HTA reviews around the world in this Pharmafocus article.
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Assessing The Impact Of MDR & IVDR On Patients
In Diagnostics World's recent article featuring commentary from ICON experts David Novotny, Angela Brown and Nicole Cowan, they discussed the need to assess the impact of MDR/IVDR on patients after the new medical device regulation is established.
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Standardised eCOA questionnaire library will speed study start-up
An Outsourcing Pharma article on the collaboration of ICON’s Mapi Research Trust and Medidata to develop a global library of pre-configured, pre-approved eCOA questionnaires to accelerate study start-up, which is being described as “a win-win-win” for all involved.
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New Frontiers
Read PharmaTimes recent article, featuring ICON expert Tom O'Leary, as he discusses his take on how the Internet of Medical Things (loMT) is evolving the patient role in pharma.
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Regulatory bottlenecks mean EU clinicians & patients could lose access to medical devices under new rules
A recent press release by Samedan LTD Pharmaceutical Publishers on ICON’s scheduled presentation to be given at The Medtech Conference 2019, ‘MDR/IVDR – What now?’, during which our experts will discuss the findings of the whitepaper ‘Higher Costs & Bottlenecks’, looking at the future implications of the new MDR/IVDR rules on the EU market.
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Making a Difference
How can we encourage more women to pursue STEM careers? Read how ICON is playing a part in this recent Conversis article.
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Hasta la vista, maybe? Terminating the Hollywood view of AI in pharma
In drug development, the success of AI depends on gathering the right data and being able to prove its authenticity when an application is subject to regulatory scrutiny. Read this Pharmaceutical Market Europe (PME) article to explore featured commentary from ICON expert Tom O’Leary on the use of AI in the pharmaceutical sector.
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The evolution of real world studies
Real world evidence is not a new concept, but its influence on drug development decision-makers continues to increase. ICON expert Bill Row discusses how life sciences companies can maximise the use of real world data to support commercial success in this Pharmaceutical Market Europe (PME) article.
