FEATURED ARTICLES

• Comprehensive Data Management For Non-Interventional Research

  Learn how your teams can embrace end-to-end clinical trial data platforms for non-interventional studies to improve user experience, boost patient engagement, ensure data quality, and achieve study success.

• Why Native Apps Trump Web Apps For Security And Performance

  Explore the advantages of native applications in clinical research, including better performance, user experience, security, and integration capabilities.

• Unify Your Data With A Centralized eClinical Platform

  Despite the challenges associated with large volumes of data, maintaining quality and regulatory compliance, and enhancing patient engagement, the solutions for managing them can be simple and efficient.

• How Can Real-World Data Benefit Your Trials?

  Clinical trial data is being supplemented with real-world data (RWD) gathered from a variety of sources. Dive deeper into this emerging trend to understand its implications for the future of clinical research.

• It Might Be Time To Move On From Your Legacy EDC

  The tools and technologies we rely on to capture and manage clinical trial data are evolving at a rapid pace. Discover how modern EDC solutions are revolutionizing the world of clinical research data management.

• Driving Customer Profitability With Enterprise Platform, Pricing

  Explore how the solutions and approaches offered by CDS can help different research stakeholders conduct more cost-efficient clinical trials in the industry's pharmaceutical, biotech, and device sectors.

• The Win-Win Wth Virtual Visits – Better Experiences, Better Data

  Discover how researchers can design studies with the needs of the patient in mind to promote faster enrollment, high engagement, and the production of more complete and accurate data.

• Leveraging Empowered Patients To Build Better Clinical Registries

  Uncover the potential of decentralized, patient-centric approaches in enhancing the efficiency and effectiveness of clinical trials and specifically, the creation of public or closed patient registries.

• Simplifying The Data Journey From EHR To EDC

  Explore how open API architecture represents a significant advancement in the integration of EHR and EDC systems, enhancing the potential of EHR data for clinical research.

• Open API Provides Better Access, Freedom To Build And Manage Studies

  Discover how the integration of all manner of data platforms ranging from central labs to CTMS and beyond can help to overcome interoperability challenges in clinical research.

• One Key To Choosing The Best eClinical Technology Vendor

  Explore why the integration of etechnologies is critical in the modernization and optimization of clinical trials, and how the right partner will ensure studies are more efficient, reliable, and inclusive.

• Collecting Trial Data From Patients In Remote Areas

  Learn how mobile technology can promote trial inclusivity and diversity, and its potential to revolutionize clinical studies, making them more accessible and representative of the population.

• The Benefits Of Mobile EDC Access

  As clinical studies become increasingly decentralized, learn why study teams need to be able to monitor the influx of data in real time to ensure the integrity and success of modern trials.

• In A Time Of Uncertainty, Reliable Partners Are Vital To Researchers

  By selecting stable and proven solution providers, uncover how researchers can ensure the uninterrupted continuity of their trials and seamlessly launch new studies.

• The Advantages Of DCTs In Diabetes Research

  By harnessing technology platforms, discover how researchers can be better equipped to design studies for novel diabetes treatments that are safer, more efficient, and more effective.

• What Does EDC Look Like In 2024 And Beyond?

  Read along as industry experts from TrialKit offer insights into the anticipated developments and challenges surrounding electronic data capture.

• Tech And Strategies For Reaching Underserved Patient Populations

  By leveraging flexible solutions, learn how sponsors can proactively address regulatory mandates while advancing the development of safer and more effective therapies for a broader spectrum of patients.

• Myth Or Fact: The Future Of Electronic Data Capture

  Explore how EDC platforms are empowering researchers to conduct efficient trials regardless of data volume, source diversity, or patient demographics.