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Latest

“Ghosting” Doesn’t Have to be So Scary for the Clinical Research Workforce

Although the phenomenon of disgruntled employees “ghosting” (also known as “quiet quitting” or “slow quitting”) their workplaces is rife with financial and ethical impacts for the life cycle of clinical research studies, interdisciplinary solutions for detecting and correcting the behavior offer some peace of mind, according to the creators behind a poster that placed in the top three among those presented at ACRP 2025. 

Clinical Trials as a Safety Net: Expanding Access for Economically Disadvantaged Populations

Clinical trials are typically seen as engines of innovation, but for economically disadvantaged individuals, they can also be a gateway to care—particularly for chronic diseases that are expensive to manage. For those living with gastrointestinal (GI) conditions like ulcerative colitis, Crohn’s disease, nonalcoholic fatty liver disease (NAFLD), or NAFLD’s advanced form, nonalcoholic steatohepatitis (NASH), clinical trials may offer access to diagnostics, treatments, and specialists that would otherwise be out of reach. 
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Events

PNW Chapter: Cautionary Tales from the Front Lines of Clinical Trials (ACRP 2025 Conference Replay)

Join the PNW Chapter for a virtual event showcasing this ACRP 2025 Conference replay session.

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FEAR: Face Everything and Rise (in Clinical Research)

David Burrow, PharmD, JD, will explore foundational principles of Quality by Design (QbD), including Critical to Quality (CTQ) factors and Risk-Based Quality Management Systems (RBQM). Participants will gain strategic insights into how to enhance trial quality while reducing regulatory uncertainty through forward-thinking approaches and practical tools.

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St. Louis Chapter: Crack the Code: A Comparison of ICH E6(R2) and ICH E6(R3) (ACRP Webinar Replay)

Join the St. Louis Chapter for a virtual event showcasing this ACRP webinar replay.

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