Dr. Bayat leads global regulatory affairs processes and activities, and also acts as clinical consultant and project manager, working closely with our clinical operations, clinical development and safety, and pharmacovigilance teams. In this capacity, he writes clinical protocols and annual reports, and contributes to writing clinical study reports (CSRs) for ongoing and completed trials across a broad range of therapeutic indications.
Dr. Bayat received his Doctorate of Medicine in 1999 and his board certification in anesthesiology in 2005. He practiced anesthesiology for a few years and then worked as a researcher at the National Institutes of Health. He has published several articles in peer-reviewed journals and presented at local and international conferences. He is currently an editorial board member for an e-book and several peer-reviewed scientific and medical journals.
His areas of expertise include:
- U.S. IND
- FDA meetings
- eCTD submissions
- Global regulatory strategic consulting