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In October 2023, the FDA issued draft guidance on Remote Interactive Evaluations of Drug Manufacturing and Bioresearch Monitoring Facilities. The document explains how the FDA

Clinical trials are designed to determine if new drugs, therapies, and medical devices are safe and effective for public use. These interventions are tested on

3 Common Barriers to Clinical Trial Enrollment + Tips for Taking Action   Despite all the good that clinical trials provide, patient enrollment is often

Recruiting patients for clinical trials is an expensive and time-consuming process, taking about 18 months on average. It’s no surprise then that many biopharmas and

Clinical trial fraud is not an uncommon problem. Though it is difficult to comprehend, it’s something that should not be ignored.  Despite the problem, there

Clinical trial safeguards have significantly improved over the last 50 years. The National Research Act, signed into law in 1974, established Institutional Review Boards (IRBs)