Featured Articles

31. How Electronic Source Data Revolutionizes Clinical Research 7/14/2023

    By increasing interoperability and embracing digital solutions, see how the research community can maximize the benefits offered by eSource, leading to improved trial outcomes and data quality.

32. Preparing Studies With eConsent For IRB Approval 6/7/2023

    Understand how eConsent can benefit trials and align with IRB ethical commitments, how to prepare your IRB submission for approval, and the future impact of large language models.

33. Unlocking The Power Of Real-World Evidence In FDA Submissions 5/15/2023

    Understand the gaps between how data is collected in real-world evidence (RWE) and randomized clinical trials (RCT) and how RWE is quickly finding ways to catch up.

34. 3 Things To Know When Using Wearables In Your Study 2/14/2023

    As wearables unleash new possibilities, the industry will need an effective strategy to utilize these useful tools. Consider these tips when incorporating wearables in a clinical study.

35. How EDCs Are Changing The Game In Clinical Research 10/17/2022

    Explore all things EDC in this article: what it is, how researchers can use it in clinical trials, its numerous benefits, and examples of how these translate into the real world.

36. EDC For Mid-Study Changes In Medical Device Clinical Trials 6/21/2022

    In this case study, discover how a company was pointed to an electronic data capture (EDC) system that was quick to adapt and easy to scale as the study changed.

37. Real-World Data Capture With EDC 5/20/2022

    This case study explores how a Ph.D. candidate partnered with Castor to develop software that seamlessly moves RWD between hospital systems and Castor’s EDC.

38. Choosing An EDC With A Robust API For DTx Clinical Trials 4/20/2022

    This white paper explores the importance of choosing an EDC with an API before starting a clinical trial.

39. Bridging Clinical Efficacy And Real-World Effectiveness In Digital Therapeutics Trials 2/7/2022

    No matter how conclusive clinical evidence is for medical treatments, developers may struggle to see precisely how their treatment performs in the real world—outside the controlled environment of the clinic or office.

40. How To Prepare An IRB Submission For A Remote eConsent Study 1/24/2022

    IRBs are increasingly supportive of eConsent solution. Even so, researchers may find themselves in need of guidance as they prepare for an eConsent IRB review.