Introduction to Affordable Care Act
On March 2010, a monumental piece of legislation was signed into law in the United States, marking a significant milestone...
Clinical data management (CDM) is the process of collecting and managing research data according to regulatory requirements to get high-quality information that is error-free...
Clinical research associates, also called clinical monitors or trial monitors, are in charge of monitoring clinical trials and assuring that regulatory, operational, and ethical...
The clinical Trial Assistant is responsible for archiving and filing clinical trial documents correctly. Assist in organizing and planning meetings (such as investigator meetings, team...
It is the duty of the clinical research coordinator to conduct trials in accordance with GCP guidelines under the supervision of the Principal Investigator...
How many types of medical scribe physicians use? Physicians use scribes to document patient-physician interaction, such as taking notes during exam time, entering data...
