Real World Data and Evidence Revolutionize Clinical Research

The FDA knows the drug approval process can often be strenuous, eating up large amounts of time and money. That’s why they’ve made a commitment to consider real-world evidence in the approval of new drug indications – a more efficient approach for manufacturers. In this piece, we’ll tell you how this is done!

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PI Perspective: Our Formula to Curb Clinical Trial Dropouts

Our team recently completed a clinical trial tasked with measuring the efficacy of a dietary supplement as an intervention for adults with an elevated blood pressure, or stage I hypertension. By employing a hybrid study model, sustaining patient engagement, and reducing resources required of the patient and study team, we successfully beat the dropout allowance.

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Poster: Achieving Diversity in Clinical Trials

Diversity in research studies is essential when conducting clinical investigations in the U.S. Learn how social media and digital clinical trials were used for recruiting participants in under-represented racial and ethnic groups. 

Look for our poster on this topic at #SOCRA2019

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An Alternate Approach to the Traditional Recruitment Nightmare

Digital patient-centric clinical trials (PCT) are often carried out in the hybrid setting (minimizing site visits and maximizing the use of a virtual site), or the site-less setting (solely using the virtual site). The pairing of a digitalized PCT with social media targeting increases the probability of successful enrollment.

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