Frequent interactions between the study team and participant help with frequent engagement, often because virtual interaction is the most convenient mode of communication for patients. In this article, I discuss my approach to five challenging real-world scenarios that I’ve encountered in the digital space.

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!

A multinational food and beverage corporation offering a line-up of brands under the diary/plant-based, and specialized nutrition categories sought to analyze the prevalence of specific functional gastrointestinal disorders (FGIDs) in infants and toddlers.

A world leading food and beverage company focused in the early-life nutrition and medical-nutrition space sought to gather real-life data from parents with infants (preterm and full-term).

A global leader in carotenoid-based dietary supplements and food/beverage products desired to understand the efficacy of one of its supplements in relieving symptoms linked with Lower Urinary Tract Symptoms (LUTS).

ObvioHealth, a digital CRO, recently completed a clinical trial solely using a virtual site model (no physical site visits) which would have likely proved futile in the traditional study format, of which requires multiple site visits. This article will further analyze the rationale behind this claim.

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.

All clinical trials require resource consumption from both the study team and participant. The following infographic will detail the differences in resources required in the digital (hybrid) model compared to that of the traditional "brick and mortar" model.

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

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.