Newsletter | June 18, 2024

06.18.24 -- Digitalized Drug Forecasting Minimizes Waste In Clinical Trial Supply Chain


Webinar: Ensuring Effective Pharmacovigilance Regulatory Intelligence with FSP Partnerships

Pharmacovigilance (PV) is a critical component of drug and medical device development and commercialization, and effective PV regulatory intelligence (RI) ensures that PV is executed accurately and cost-effectively. Join us to examine several PV RI capabilities that differentiate top-tier FSP PV partners from other service providers and discover what it takes to stay on top of constantly changing regulatory requirements. Click here to learn more.


Digitalized Drug Forecasting Minimizes Waste In Clinical Trial Supply Chain

Why should pharma companies strive for more sustainable clinical trials? And how can digitalizing drug forecasting reduce waste in the supply chain? J&J Innovative Medicine's Kristel Rens explains.

8 Ways Medical Device Clinical Trials Differ From Drug Trials

Delve into the nuanced disparities between medical device and drug clinical trials with eight critical differentiators shaping regulatory pathways and patient safety.

How Health Information Technology Is Transforming Human Lives

Follow along as authors take a closer look at how these advancements are not just revolutionizing healthcare but also instilling hope for a brighter and healthier future.

Build Better Studies Faster: 3 Advantages Of Mobile eClinical Platforms

Embrace the digital revolution in clinical research with advanced eClinical platforms that expand reach, enhance efficiency, and streamline processes, revolutionizing your trials and work-life balance.

How Technology Can Empower CAR T-Cell Therapy Clinical Trials

Explore how innovative technologies are pushing advancements in CAR T-cell therapy, enhancing patient outcomes, and streamlining trial processes.

Vaccine Trial Sees >90% eCOA Adherence

Here, we addressed vaccine trial challenges and drove remarkable success, achieving over 90% adherence to eCOA, ensuring active engagement from participants, and yielding consistent trial data.

When QuickBooks Leaves Your Life Sciences Venture Struggling

Is QuickBooks keeping pace with your life sciences venture? Learn the signs it's time to move beyond and adopt tailored solutions for growth, compliance, collaboration, security, and automation.

How eConsent Delivers Value For Sponsors

Review data substantiating experiences with electronic informed consent to better understand their positive impact on the outcomes of clinical trials.

Streamline Data Collection, Management, And Compliance

Empower personnel by seamlessly capturing and overseeing data, facilitating remote workflows, and eradicating redundant processes with Advarra's eSource + EDC.


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  • Clinical Trial Technology (Tuesday)
  • Decentralized Trials | Trial Management (Wednesday)
  • Outsourcing Models | Regulatory & Compliance (Thursday)
  • Clinical Data Management & Analytics | Trial Monitoring (Friday)

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