Sponsors of clinical trials in the United States have a regulatory responsibility under 21 CFR Part 312.50 to monitor the progress of clinical studies. Historically, Sponsors performed in-person ...

As the research coordinator for a large cardiology practice, Sandy Maddock saw the good and the bad ways to conduct clinical trials for medical devices and drugs being developed to help patients.

Over the last 10 years, clinical trials have changed substantially in response to increasing globalization and study complexity, along with new technological capabilities and industry guidelines 7.

Noninvasive haemoglobin monitoring has emerged as a transformative technique in clinical settings, providing continuous, real‐time assessments of blood haemoglobin levels without the need for repeated ...

ORLANDO, Fla.--(BUSINESS WIRE)--Dolbey, the developer of the KLAS Category Leader for Computer-Assisted Coding software, has partnered with Maxim Healthcare Services, an established provider of home ...