Digital patient profiles and real-world data enhance oncology trial design, patient recruitment, and reduce trial failure risks. Phesi's platform aligns trial designs with real-world data, minimizing ...

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

Handling sensitive patient data is a critical responsibility for organizations involved in clinical trials. To meet regulatory requirements, many rely on SDTM mapping—a process that converts raw ...

Traditional clinical trial data are pseudonymized data, and these data may not contain information on a patient that directly identifies them, like a name, address, or phone number. However, ...

Objective: To understand patient portal engagement stratified by patient characteristics among adults 50 years and older with at least 1 common chronic medical condition using electronic health ...

Patient access to innovative new therapies requires us to reimagine the supply chain and how it integrates advanced technologies.

Remote Patient Monitoring (RPM) uses digital tools like wearables and sensors to track patient health data outside the clinic. Studies show RPM can reduce hospitalizations and ER visits, especially ...

Health care data exists in many forms, from medical records held in health care facilities to information captured through daily routines and lifestyle choices. This includes vital signs, medication ...

Unlike other sectors, US healthcare businesses must reconcile cost-saving strategies with stringent compliance obligations, especially when patient data crosses national borders or is accessed ...