Dive into the highs and lows of 2023 in clinical research! Explore groundbreaking studies, regulatory milestones, and the latest in digital therapeutics in this year’s top news recap.
Uncover clinical trial design and execution solutions for collecting high-quality data for approvals.
Learn about re-consent challenges, regulatory insights, and the role of eConsent in streamlining informed consent processes.
Unlock key clinical trial supply chain optimization strategies to ensure efficient logistics, reduce waste, and streamline operations.
Explore how to keep your clinical trial data safe, secure, and protected in three key steps.
Navigating the unique complexities of rare disease research is challenging. Discover key strategies and solutions to support participants and reduce overall burden.
Uncover solutions for oncology trial success: conquer enrollment and retention obstacles, expedite timelines, and navigate global supply chains.
Learn unique approaches to study design and supply chain management to better navigate the complex landscape of rare disease clinical trials.
Understand how the European MDR (EU MDR) will impact medical device manufacturers and what you can do to prepare.
Data management in clinical research is at an inflection point. Learn what you can do to create more accurate, high-quality clinical trials.
Digital data capture, such as electronic data capture (EDC), ePRO, and eConsent, create patient centricity and enable accurate data collection.
Understand the challenges with source data verification and learn how eSource affects clinical trials and improves data integrity.
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