Welcome to the Law Office of Shannon O'Barr Sausville

Navigating the hurdles involved in human subjects research, FDA product approval and the health care industry in general is challenging, with a constant stream of changes to regulations. Ms. Sausville combines her background and experience in science, public health and the law to support your specialized needs.  Working as a solo practitioner, Ms. Sausville brings personal attention to your project, whether you are just starting on the regulatory process for a new drug or only need help with an isolated challenge along the pathway.

Ms. Sausville can assist you with issues including but not limited to:

  • IND / IDE submissions
  • FDA 483 letters
  • Informed consents
  • Clinical trial contracts
  • IRB submissions
  • Clinicaltrials.gov compliance
  • Human subjects research compliance
  • Clinical trials best practices and standard operating procedures
  • Physician employment contracts


Address : 3311 Pocahontas Drive
Edgewater, MD 21037
Phone : (301) 237-7901
Fax : (443) 203-6721
Email : Shannon@SOSausvilleLaw.com