Newsletter | March 7, 2023

03.07.23 -- Questions Sponsors Should Ask When Selecting Tech Vendors For DCTs

Webinar: Unlock the Power of Data Review and Collaboration: Maximizing Trial Success

Join us to discover how leveraging dynamic workflows to review, query, track, and collaborate cross-functionally in a clinical trial can result in better trial conduct, potential study amendments, and evolving clinical strategies. Click here to learn more.

Clinical Trial Technology
Questions Sponsors Should Ask When Selecting Tech Vendors For DCTs

Elevar Therapeutics’ Jennifer Lee, RSM US’s Steve Kemler, and Janssen Clinical Innovation’s Bert Hartog recently discussed the challenges of new technology implementation. Here, Lee provides her top questions sponsors should be asking themselves before choosing a technology vendor.

Effective Use Of IRT In Decentralized And Hybrid Clinical Trials

Interactive response technology is likely to play an increasingly significant role in addressing complex challenges in drug management and distribution. Learn how IRTs can help trial sponsors manage the distribution of medications, forecast trial supply, and integrate workflows with other platforms.

3 Key Functions Your eTMF Needs To Meet New EMA Regulations

The European Union Clinical Trial Regulation No. 536/2014 introduced the most significant changes to the processes for clinical trial applications in the last 15 years. Consider three key functions that an electronic TMF must have to achieve compliance and maintain organizational success.

The Secret Sauce In Successful Clinical Trial Payments Programs

More than 80% of sites surveyed want to get paid in 30 days, and many clinical technology companies offer specialized software solutions to address the site payments process. However, these systems still require a large effort by the sponsor to operate. What is the secret sauce for success?

The False Economy Of Paper Diaries In Clinical Trials

While paper diaries may appear cheaper, there are hidden costs that make a digital eCOA solution much more affordable in your clinical trial. Find out how these two approaches compare in terms of cost.

Fast-Tracking Clinical Trials With Automated Source Data Capture

Learn how developments in EHRs and eCRFs are reducing the time, cost, and effort required to access quality data needed to evaluate new and repurposed therapies.

ClinCard Tax Toolkit

ClinCard's Tax Toolkit supports research sites and sponsors in remaining IRS tax compliant while maintaining confidentiality and privacy.

CTMS Benchmarking And Market Dynamics

ISR’s CTMS Benchmarking and Market Dynamics (3rd Ed.) aims to tackle CTMS by helping providers and sponsors better understand current trends surrounding this tech while anticipating future ones.

Patient Data: The Backbone Of Your Clinical Trial

In clinical trials, data capture is typically centered around patients’ experiences with a drug. Discover why electronic clinical outcome assessments (eCOAs) are essential to patient data capture.

Unlock Additional Capabilities For Your Next Clinical Trial

Gain insight on how a single point of entry can improve patient and site experience by offering best-in-class eCOA, consent management, and patient engagement solutions.

2023 PDA Advanced Therapy Medicinal Products Conference

The 2023 PDA Advanced Therapy Medicinal Products Conference, June 7-8, in Baltimore, MD, will focus on the theme, "Navigating through CMC Challenges." This popular conference will offer a forum for sharing best practices and learning from the experts how the industry is applying novel approaches to a wide variety of topics relating to cell and gene therapies. Register now!

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  • Clinical Sites | Patient Centricity | Patient Recruitment (Monday)
  • 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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