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Whether unstructured patient diaries will be part of future clinical trials depends on three main factors, including answers around added value.

Streamlining electronic clinical outcome assessment and patient-reported outcome processes can aid in decreasing timelines.

The current clinical development model is shifting toward a generative AI-augmented proactive approach supported by real-world data for real time evidence.

Spearheaded by disease foundations, the creation of clinical registries is streamlining data collection and driving informed decisions.

Maximize your Study’s Potential: How Expert Recommendations on Data Collection, Data Flow, Standards and AI can Transform Outcomes
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Webinar Date/Time: Thursday, May 9th, 2024 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST

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Webinar Date/Time: Tuesday, May 7th, 2024 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST

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Webinar Date/Time: Thursday, May 2nd, 2024 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST

As clinical trials continue to advance and evolve to include real-world data, their success is becoming ever more dependent on the quality of data.

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Webinar Date/Time: Tuesday, April 30, 2024 at 11am EDT | 8am PDT | 4pm BST | 5pm CEST

Because of drastic changes in the clinical trial space, there is a need for advancing and streamlining design through risk-based methodologies and innovations.

Although there are much larger problems in clinical research, storing obsolete study records is a totally unnecessary cost.

Industry leaders discuss how technology can help companies adapt to the regulatory changes and accomplish their DE&I goals.

Exploring ways to boost the adoption of eCOA provider-specific libraries—an often-frustrating migration process, but one with significant payoffs in simplified workflows and reduced timelines.

The FDA has taken a clear position with Project Optimus in shifting toward more progressive tailored approaches while rejecting antiquated study designs to evolve clinical trial strategies to better align with newer drug classes.

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Webinar Date/Time: Tue, Mar 26, 2024 11:00 AM EDT

Agency reports concerns amid an increase in submitted data that has been fabricated, duplicated, or unreliable from third-party laboratories.

Many companies have implemented new technologies and are adopting clinical trial models that are more patient-centric.

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Webinar Date/Time: Thursday, March 14th, 2024 at 11am EDT | 8am PDT | 3pm GMT | 4pm CET

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Webinar Date/Time: Tuesday, March 12th, 2024 at 12pm EDT | 9am PDT | 4pm GMT | 5pm CET

Breakout session at SCOPE Summit 2024 discusses the potential use of artificial intelligence to improve clinical trial strategy generation.

Addressing challenges with eCOA at the site-level.

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Webinar Date/Time: Wed, Mar 27, 2024 11:00 AM EDT

Leveraging a “diversity by design” approach can build patient narratives and optimize protocols from the onset.

Recent study tests the ability of machine learning to effectively classify patient safety event reports.














