FEATURED ARTICLES

• eCOA In Oncology Trials: A Tool To Simplify

  Accurate quality of life data is critical in oncology. eCOA unified with IRT streamlines trials, improves data collection, and enhances site user experiences across therapeutic areas.

• Why Real-Time eCOA Data Matters More Than Ever

  Real-time eCOA data enables faster eligibility decisions, proactive issue alerts, and streamlined operations by unifying data, improving precision, responsiveness, and trial execution efficiency.

• A Merger Supporting A More Seamless Trial Experience

  Clinical trials don’t have to be so complex. Jagath Wanninayake shares why focusing on time-sensitive moments—and not everything at once—can drive better outcomes and how a recent merger supports that shift.

• Increasing Efficiency And Reducing Drug Waste

  Discover how streamlined clinical supply chain management helped accelerate study timelines, reduce costs, and support global treatment delivery through a strategic technology partnership.

• Accelerating Study Startups: Drive Efficiency From Protocol To Go-Live

  Speed up trial launches and maintain predictable timelines by leveraging a modern, integrated approach to eCOA setup that reduces complexity.

• Understanding Decentralized Clinical Trials: FDA vs. EMA Fundamentals

  Designing a global decentralized clinical trial requires understanding the differing FDA and EMA approaches to trial models and informed consent.

• Managing Drug And Data Requirements In Decentralized Clinical Trials

  Running a global decentralized clinical trial requires a deep understanding of the differences in FDA and EMA requirements for investigational products and patient data.

• 5 Essential Steps To Implementing Decentralized Clinical Trials Globally

  Running a global decentralized clinical trial requires a strategy that balances the FDA's focus on technology accessibility with the EMA's emphasis on validation and comprehensive documentation.

• Sustainable Clinical Trials Through eClinical Innovation

  Clinical trials are essential to advancing medicine, yet they carry significant environmental costs. Inefficiencies not only drive emissions but also risk drug shortages and trial delays, and clinical technology solutions offer a pathway to more sustainable research.

• Honoring Patient Altruism: Empowering Trial Participants With Better Technology

  Simplifying participation honors patient altruism, improves engagement, and strengthens the quality of trial data, ultimately advancing medical innovation.

• How Cara Therapeutics Increased Compliance And Reduced Study Team Burden

  Delve into the partnership that helped Cara Therapeutics achieve a significant milestone in their clinical research efforts to transform the lives of chronic pruritus patients.

• What Is The Suvoda Platform?

  If you're ready to streamline your clinical trials and deliver better outcomes for all stakeholders, explore how the Suvoda Platform can transform your trial experience today.

• Drive Innovation In Clinical Trial Software: 3 Trends You Need To Watch

  The clinical trial landscape is undergoing a transformative shift as technology increasingly shapes study design and execution. Explore three pivotal trends that are driving this evolution.

• Managing Risk And Regulation In Clinical Trial Technology

  Now is the time to evaluate your current risk management framework. Take action today to strengthen your safeguards, tailor your risk assessments, and prioritize transparent patient engagement.

• Recent Updates To The Declaration Of Helsinki Affecting Clinical Trials

  The World Medical Association (WMA) has announced a significant, rare update to its cornerstone ethical document, the Declaration of Helsinki, which guides medical research involving human participants.