The term “special population” exists to protect certain vulnerable patient groups that require additional consideration as it pertains to clinical research, including women, pediatrics, and the elderly.
Regulatory agencies require clinical trial sponsors to present a summary of safety and effectiveness data by demographic subgroups, for age, gender, and ethnicity – because one size does not fit all.
In this webinar, we will explore these different patient populations, outline the challenges to trial recruitment and retention, and overview the regulatory efforts underway to ensure inclusive research.