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Regional inequalities threatening Europe’s biosimilars market

European Pharmaceutical Review

This is based on research from a report published in April this year by IQVIA. Additionally, overall affordability of biologics limits the number of patients who can access these advanced treatments in Eastern Europe, the authors explained.

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QMS market to value nearly $4b by 2030

European Pharmaceutical Review

This is affecting a considerable percentage of their total cost structure, the authors stated. Key factors such as the growing emphasis on process deviation records by regulatory authorities to analyse overall process quality primarily are contributing this growth.

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Improving trial predictability: leveraging AI-powered analytics to guide trial design, strategy, and operations

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About the authors. Natalia Kotchie, vice president, R&DS Applied Data Science Center, IQVIA. Natalia leads the Applied Data Science Center (ADSC) for R&D Solutions at IQVIA, which is responsible for data and analytics to support clinical trial strategies, including trial design and feasibility. †Ther Innov Regul Sci.

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Innovative Medicines Fund and the opportunity for ICSs to mobilise NICE approvals

pharmaphorum

VP Strategic Planning, IQVIA UK & Ireland and North Europe. As VP, Strategic Planning for IQVIA, Angela works closely with UK Government, the NHS, the Pharmaceutical and Biotech Industry and Patient Organisations on pioneering collaborations that will improve NHS patient access to clinical trials, RWE studies and innovative medicines.

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Nine for 2023, part three: thriving or surviving?

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In this final instalment of IQVIA EMEA Thought Leadership’s Nine for 2023 three-part series, focusing on issues that will change the direction of healthcare and the pharmaceutical industry this year, three key competitive issues for pharmaceutical companies in 2023 are assessed. She holds a degree in biochemistry from Oxford University.

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It’s time get real with healthcare’s commitment to net zero

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IQVIA examined the top 100 companies by global sales revenue (IQVIA MIDAS) and extracted data on commitments and progress (Figure 1). About the author. Here is what was found: Less than half of top 100 companies have reported time-bound commitments.

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Key operational considerations to optimise decentralised clinical trials

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IQVIA conducted a thorough analysis of 12 global DCT studies across three therapeutic areas and seven indications to compare DCTs’ value to key stakeholders with traditional trials. About the author. Patricia Salter, Head of Global DCT Operations, IQVIA.