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As the COVID-19 pandemic continued, clinical researchers looked for ways to safely continue clinical trials to progress. With FDA guidance, trials were able to resume with the help of technology.

In our latest guide, we break down what you need to know before conducting a remote trial.

Other Guides

  • Envisioning the Next Generation of EDC Systems: Creative Innovations in Clinical Trial Data Collection

    As Electronic Data Capture (EDC) systems continue to advance, it’s essential to think beyond the current functionalities and explore more creative and futuristic ways these systems could transform clinical trials. This blog post proposes imaginative yet plausible advancements that could redefine how EDC systems support clinical research, making trials more efficient, adaptive, and patient-cen...

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  • Navigating the Ethical Terrain of Genetic Testing in Oncology

    Genetic testing in oncology offers unprecedented opportunities for early detection, personalized
    treatment, and better patient outcomes. However, the rapid advancement and integration of genetic
    testing into cancer care also bring to light significant ethical considerations. This blog post explores the
    ethical issues associated with genetic testing in oncology, such as privacy...

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  • Real-World Evidence: The Game Changer in Clinical Research

    The era of one-size-fits-all medicine is gradually coming to an end, making way for a more personalized
    approach to healthcare. Personalized medicine, also known as precision medicine, tailors medical
    treatment to the individual characteristics of each patient. This approach not only considers the patient's
    genetic makeup but also factors in lifestyle and environment, ensuring...

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