In today's healthcare environment, securing regulatory approval is only the beginning. The real challenge lies in ensuring ...

Representative clinical studies are important as diseases and medicines can affect people differently depending on their age, sex, and race and ethnicity. According to the Food and Drug Administration ...

Since 2003 the NCI's Health Information National Trends Survey has collected nationally representative data about the American public’s knowledge of, attitudes toward and use of health-related ...

During months of direct research, the Sequoia Project's Consumer Voices Workgroup facilitated discussions and polls focused on patient and provider experiences using electronic health record-based ...

How can better use of patient data improve health equity? Adam Mariano, Esq., MSPH, senior director, Product and Strategy, Integrated Health Practice at IQVIA, discusses with Evidence-Based Oncology ...

BOSTON--(BUSINESS WIRE)--Care Access, the world’s leading decentralized research organization (DRO), today announced its expanded partnership with global biopharma leader Eli Lilly and Company (Lilly) ...

Sociodemographic Inequities in Telemedicine Use Among US Patients Initiating Treatment in Community Cancer Centers During the Ongoing COVID-19 Pandemic, 2020-2022 The COVID-19 pandemic expanded ...

Discusses Zydus Collaboration, Global Manufacturing Expansion, and Patient Access Initiatives January 28, 2026 4:00 PM ...

WASHINGTON, D.C. (WNCT) — Congressman Greg Murphy (R-NC), Adam Gray (D-CA), and Neal Dunn (R-FL) introduced the Protecting Patient Access to Cancer and Complex Therapies Act. This legislation would ...

Providing parents with access to their child’s healthcare information is not a new legal requirement, but given recent ...