The flowchart and steps below outlines the best practice for processing industry-written and sponsored clinical trials at UAB. There are many small steps in each of the larger defined steps (see flow ...

The Food and Drug Administration (FDA) development and approval process for drugs and medical devices involves multiple phases that ensure the safety and effectiveness of products before and after ...

Traditional trial start-up workflows often follow a sequential path, from feasibility to contracting, then regulatory ...

The use of Artificial Intelligence (AI) and Machine Learning (ML) in clinical research is rapidly evolving, offering a glimpse into a future where medical innovation is driven by data-driven ...

After a tumultuous several years for the Food and Drug Administration, the agency will soon get a new leader in President Biden’s pick, Dr. Robert Califf. In the wake of a pandemic that exposed ...

Clinical trials are an essential step in medical science; they are the key. They serve to answer questions about the safety and efficacy of new treatments, drugs, and interventions. In this post, we ...

Clinical Trial Media (CTM) works with the world’s leading pharmaceutical companies to drive participant recruitment and retention through all stages of clinical research. Over the past 25 years, the ...

Academic research is a challenge in low- and middle-income countries. Pertinent questions for local populations remain largely unaddressed. Countries and regions are heterogeneous in terms of research ...

The flowchart and steps below outlines the best practice for processing industry-written and sponsored clinical trials at UAB. There are many small steps in each of the larger defined steps (see flow ...