Most healthcare organizations already have access to much of the data they need, but the challenge is operationalizing it ...

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 ...

Ten non-profit researchers will receive full independent access to the data, analytical tools, and technical support at no ...

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 ...

Doing more with less has become a new normal in healthcare, driven by industry-wide workforce reductions and budget cuts. This pressure is only amplified as health infrastructure faces mounting stress ...

Clinical trial recruitment failures have persisted for decades, yet most sponsors still plan studies using the same basic approach: look at historical recruitment rates, identify sites with patient ...

Incorporating patient voice early can reduce burden through fewer visits, simpler procedures, and selective decentralization while maintaining trial objectives. Engagement failures commonly stem from ...

You arrive at the scene to find a patient struggling to breathe. They can’t speak clearly, no family is present, and no one knows their medical history. What medications are they on? Do they have life ...

Madam, which medicines do you take? I'm sorry, but I can't access your information on my computer”, said the gynaecologist (TA). This conversation took place on March 10, 2026, at a referral hospital ...

This retrospective analysis explored the impact of infertility health benefit design on the use of infertility medications and procedures and pregnancy outcomes. Objectives: Assisted reproductive ...