Katherine Szarama has been named acting director of the FDA's Center for Biologics Evaluation and Research, overseeing vaccines, gene therapies, and blood supply regulations. This shift is crucial for developers as it may influence regulatory approaches and decision-making processes in biotech and pharma sectors. Watch for changes in the review and approval timelines under Szarama’s leadership.
Read the full article at STAT Pharma
Want to create content about this topic? Use Nemati AI tools to generate articles, social posts, and more.





