If you missed this critical webinar on how to transform your site partnerships and drive operational success in patient-centric trials, you can catch up now with on-demand! Watch now and discover how to evolve your trials through the digitalization of clinical research. https://bit.ly/3GFybYD #clinicalresearch #clinicaltrials #patientcentric
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If you’re struggling to understand the revised rules around the publication of clinical trial information and documents now that the EMA has released more information, IQVIA’s Clinical Trial Regulatory Management (CTRM) team can help you to make sense of the changes – and the benefits they bring. Learn more about the implications of the new rules. https://bit.ly/3A6eYj3 #clinicaltrials #regulatory
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Catch up with our recent expert-led webinar to explore the latest advancements in FSP remote monitoring capabilities. Learn how to address sponsor oversight, comply with regulatory requirements, and identify and resolve issues faster using next-generation approaches. Watch now. https://bit.ly/3Yse6yC #FSP #remotemonitoring
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The challenge in proving the efficacy of an HIV vaccine lies in the ability of PrEP to reduce overall rates of new infection. This fascinating insight brief, proves the efficacy of a vaccine in the era of PrEP will be near impossible without an accepted correlate of immunity. https://bit.ly/4f5Cdsv #HIV #Vaccines
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With complex protocols characteristic of CAGT trials, working with specialized entities can help CROs find patients and address complex logistics. From patient recruitment and retention to country and site selection, IQVIA’s VP and Global Head of Cell and Gene Therapy Diego Correa walks us through the four key elements that are essential to the success of CAGT development programs. Read more. https://bit.ly/401oIWu #CAGT #patientrecruitment #siteselection #clinicaltrials
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With over two decades of Gastroenterology and Hepatology experience, our team of therapeutic experts have built end-to-end capabilities, expertise, and data resources across more than 200 clinical trials over the past two decades. From IBD and MASH, to Celiac Disease and Gastroenteritis, discover just how far our expertise takes us. https://bit.ly/487GGsc #gastroenterology #hepatology
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IQVIA Targeted Site Analytics empowers you with insights that often go undetected with standard analytics – summarizing exactly where, when, and why your site is at-risk, and integrating insight-driven risk mitigation into your existing trial model. Download the fact sheet to uncover the power of IQVIA’s centralized site-specific risk detection & mitigation. https://bit.ly/3BPyild #analytics #centralizedmonitoring
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Join IQVIA’s Sharon Hughes and Rachel Freeman for an insightful webinar on antimicrobial resistance (AMR), tailored for experts in clinical development. Register now. https://bit.ly/4eIZEYH #AMR #antimicrobialresistance
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SCOPE Europe is your chance to step into the future of clinical operations excellence. With our experts in attendance, we can’t wait to explore the latest trends in clinical trial innovation, planning, and operations with fellow industry leaders. If you’re heading to the event, schedule a meeting or come and see what we’re up to at IQVIA Booth 1. https://bit.ly/3NrvLjC #clinicaloperations #clinicaltrials
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In a highly regulated and dynamic market, clinical trial professionals are constantly having to navigate challenges, all while managing practical constraints and maintaining the highest ethical standards.
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In this compelling article for Applied Clinical Trials, IQVIA’s David Alsadius, Sergio Sánchez-Gambetta, and Matt Simmons discuss several exciting areas of progress in oncology R&D. Our experts outline what sponsors, clinical research organizations, regulators and other key stakeholders will need to keep in mind for successful drug development. Read their insights in full. https://bit.ly/4eI622w #clinicalresearch #drugdevelopment #oncology
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