Register Now - Beyond Recruitment: The Future of Patient Site Engagement in Oncology Clinical Trials

IQVIA

Articles by IQVIA

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Learn more about global regulatory acceptance of real-world evidence in a regulatory submission. Understand how to identify opportunities to incorporate real-world Evidence in your submission package. Live: Tuesday, Apr. 7, 2020 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST On demand available after airing until Apr. 7, 2021. Register free

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Enter a new era of clinical development planning. Use the power of “big data” and machine learning to generate more accurate plans that embrace uncertainty. Learn how to improve your development planning strategy while reducing trial costs and durations. Live: Thursday, Jan. 30, 2020 at 11am EST | 10am PST | 4pm GMT | 5pm CET On demand available after airing until Jan. 30, 2021. Register free

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Regulatory requirements continually change, requiring the use of new innovative approaches, including technology advancement and process automation. Join us and take advantage of lessons learned from your peers to eliminate bottlenecks and leverage up-to-date regulatory intelligence to mitigate risks. Live: Tuesday, Dec. 10, 2019 at 11am EST On demand available after airing until Dec. 10, 2020. Register free

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• Using up-to-date data ensures budget accuracy for clinical trials. • Budgets require tools for cost savings, defendable processes, and more. • GrantPlan enables budgeting teams to keep costs at fair market value.

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Using AI/ML and advanced techniques in clinical development is more than just hype – it is greatly enhancing clinical trials today! Learn how pharmaceutical firms are realizing the benefits of better study design, faster recruitment, automated safety approaches and more informed, faster decision-making with risk-based and centralized monitoring. Live: Tuesday, Oct. 1, 2019 at 11am EDT On demand available after airing until Oct. 1, 2020. Register free: Register free