The Food and Drug Administration (FDA) will soon require clinical trial sponsors to submit a plan for improving diversity among clinical trial participants. While...
The FDA 505(b)(2) regulatory pathway for drug approval, which allows applicants to use existing safety data as evidence, continues to grow in popularity. Innovators...
The notion that a quality clinical trial should be conducted in highly specialized and experienced study centers with tight oversight of patients is becoming...
The ongoing digital revolution in clinical trials has created a daunting new task for the sites conducting the research: managing all the technology required...
Clinical trial sponsors are constantly trying to balance different goals and demands. Ensuring data quality is key, yet clients also seek to recruit diverse...
Contract manufacturing organizations (CMOs) and contract development and manufacturing organizations (CDMOs) are biotechnology firms that offer a variety of services to pharmaceutical and biotechnology...
Human life was transitory before the discovery of modern medicine. Unseen risks in the form of sickness and medical disorders abound in the environment....
Until relatively recently, vision had been considered an attribute of animates only. The ImageNet challenge provided a showcase for artificial intelligence (AI) tools for...
The Food and Drug Administration (FDA) will soon require clinical trial sponsors to submit a plan for improving diversity among clinical trial participants. While...
Antibiotics have revolutionized human medicine in the twentieth century. Deadly diseases such as streptococcal pneumonia or gangrene became curable, and also other advances of...
The FDA 505(b)(2) regulatory pathway for drug approval, which allows applicants to use existing safety data as evidence, continues to grow in popularity. Innovators...
A powerhouse group was created with the goal of getting ASTM to adopt standards for SIJ fusion devices.
Accurate, repeatable, and reproducible—that’s the mantra we’ve...