Avoid these 5 real-world data pitfalls when planning your patient registry, cohort study

Vineet Bhatt28 Sep, 2024Technology

Traditionally, major bottlenecks occur during study startup, eligibility screening, the informed consent period (including assent in pediatric studies), and patient travel to the clinical site(s). Researchers eager to get the ball rolling on their study can save time and ease logistical burdens by stopping data gridlock before it begins.