Featured Articles

61. How To Avoid Remote Site Monitoring Failures 9/8/2020

    Remote site access, monitoring, and SDR/V are essential to mitigate COVID-19 disruptions to clinical trials in the short-term and to accelerate the research industry in the long-term. However, one doesn’t have to look far to find failed attempts at remote site monitoring. As an industry we are positioned – and poised – to get it right this time around, this article explores insights as to how to avoid these failures.

62. 9 Ways Your Technology Vendor Should Support Global Compliance In Clinical Research 9/8/2020

    As the number of global clinical trials continues to rise it is important to understand the global compliance requirements needed for technology being utilized by your organization. This knowledge will empower you to select vendors that adhere to these requirements and support your ability to take on studies or scale participating sites regardless of their geolocation.

63. Simple SOP Updates Every Research Site Needs To Succeed At Remote Monitoring 9/8/2020

    Today’s crisis climate is creating a dichotomy in clinical research. As a result, sites are closing, medical facilities are enforcing access restrictions, and there are constant delays or stoppage of non-essential studies. On the other hand, this health crisis is highlighting the critical need for clinical research due to ongoing COVID-19 trials. As a result, clinical researchers are asking questions and seeking workarounds to continue operations in response to site-specific adjustments. One central issue has surfaced — how do we continue to maintain compliance when working from home?

64. Impact Of COVID-19 On Clinical Trial Operations: How Leaders Are Changing Their Transformation Agendas 9/8/2020

    COVID-19 radically disrupted clinical trial operations and forced an acceleration of the transformation agendas leaders had in place pre-crisis. While the acceleration of pre-crisis transformation agendas in clinical trial operations will be measurable, it will not leap to a 10+ year horizon. This blog takes a deeper dive into these changes and how it will affect the industry.

65. Complete Buyer's Guide To The Modern Electronic Trial Master File (eTMF) 9/8/2020

    Implementing an eTMF is critical for Sponsors and CROs that want to reduce burden, increase study capacity, and enable more trials. However, many organizations are not equipped with a modern solution to realize the full benefit and future proof operations. This guide serves as an in-depth overview of how a modern eTMF solution can impact your organization and the steps you can take to prepare.

66. Harness Site-Based eISF For Remote Site Access And Monitoring 9/8/2020

    The ability to access and collaborate with a research site is essential to the success of every study. A disconnected mix of on-site visits, email communications, and portals restrict site access and document exchange for Sponsors and CROs alike. Read how remote site access, source document review/verification and streamlined workflows transforms essential clinical trial processes.

67. Study Start-Up Checklist For Digital Clinical Trials

    Read how five Florence employees with clinical research backgrounds came together to craft a checklist designed to walk sites through the process of tech-enabled study start-up.