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EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
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Middle East & Africa
EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
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EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more -
Middle East & Africa
EMEA Thought Leadership
Developing IQVIA’s positions on key trends in the pharma and life sciences industries, with a focus on EMEA.
Learn more
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Impacting People's Lives
"We strive to help improve outcomes and create a healthier, more sustainable world for people everywhere.
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Harness the power to transform clinical development
Reimagine clinical development by intelligently connecting data, technology, and analytics to optimize your trials. The result? Faster decision making and reduced risk so you can deliver life-changing therapies faster.
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Generate and disseminate evidence that answers crucial clinical, regulatory and commercial questions, enabling you to drive smarter decisions and meet your stakeholder needs with confidence.
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Orchestrate your success across the complete compliance lifecycle with best-in-class services and solutions for safety, regulatory, quality and medical information.
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IQVIA Decentralized Trials deliver purpose-built clinical services and technologies that engage the right patients wherever they are. Our hybrid and fully virtual solutions have been used more than any others.
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WE’RE HIRING
"Improving human health requires brave thinkers who are willing to explore new ideas and build on successes. Unleash your potential with us.
SEARCH JOBSOverview: With more than 80% of oncology therapies in development being precision medicines, the demands for data and evidence to support clinical development and commercialization have changed. We are seeing new challenges across the development lifecycle, including clinical trial site selection and recruitment and finding the right real-world data to support various evidence needs. With testing often limited to known and actionable biomarkers, there are additional hurdles to bring these drugs to patients once approved. In this session, we would like to discuss the era of precision oncology: testing practices, development needs, data hurdles, and how we can overcome these obstacles.
The IQVIA Institute will assemble a mixed panel to give a holistic view from the perspective of patient, pharma (large/small) and regulator. This interactive discussion will explore the challenges, key levers, and scenarios for precision oncology trials to find the right data for the right decision at the right time, thus ensuring all patients benefit from precision therapies. The panel will seek to address these topics:
- Precision medicine—is the hype too good to be true or is this the future?
- How do testing requirements impact a patient’s ability to participate in a clinical trial?
- Given the complexities and additional burden, how do we communicate the importance of precision medicine trials and ensure prioritization by stakeholders?
- Do we need to challenge the current data access/usage approaches to support evidence generation from trials that support drug launches? Is there a need for ‘co-opetition’?