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Xtalks, Online
2024-10-21
The clinical development landscape has become increasingly complex, evolving rapidly in response to post-pandemic demands, hybrid trial designs and the growing use of real-world data (RWD). These changes are driving the need for sponsors to conduct faster, more efficient trials while managing a rising volume of clinical data.
Adding to this complexity, ongoing trials across multiple therapy areas, many of which are outsourced to contract research organizations (CROs) can lead to sponsors having lower visibility over trial performance and progress. As regulatory expectations continue to evolve, particularly with the US Food and Drug Administration (FDA)’s review of International Council for Harmonisation (ICH) E6 (R3) guidelines, sponsors are under increased pressure to maintain oversight and ensure the quality, safety and integrity of their trials.
In this webinar, IQVIA SMEs, in partnership with the Everest Group Industry Analyst, will dive into the pressing challenges sponsors face in clinical data management today. They will explore how an end-to-end unified clinical data and analytics (D&A) platform can offer a solution to sponsor challenges by acting as a single source of truth, offering a centralized hub to manage all aspects of their clinical trials in real time.
This webinar will also provide an opportunity for clinical trial stakeholders, including biopharma companies, MedTech enterprises and CROs to learn how they can harness the power of a unified D&A platform to navigate the complexities of modern clinical trials. The speakers will also delve into practical aspects that sponsors consider when deciding whether to deploy a clinical D&A platform, like evaluating return on investment (ROI) and key performance indicators (KPIs) to measure success.
They will also explore the role of next-gen technologies such as artificial intelligence (AI) and generative AI and how they are leveraged by these platforms to automate repetitive tasks and extract valuable insights for clinical trials.
Register for this webinar today to discover how clinical data management can be optimized to help sponsors navigate the complexities of modern clinical trials, improve oversight and ensure data quality.
Keywords: Clinical Research, CRO, Data Analytics, Clinical Data, Regulatory, Analytics, Data Management, Clinical Data Management, Commercialization/HEOR/Market Access
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Organized by:
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Xtalks |
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Invited Speakers:
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Nisarg Shah, Practice Director, Everest Group
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Deadline for Abstracts:
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2024-10-21
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Registration:
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Free Registration
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E-mail:
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tristan@xtalks.com
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