Welcome to the Law Office of Shannon O'Barr Sausville

Navigating the regulatory hurdles involved in human subjects research, FDA product approval and the health care industry in general is challenging. 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
  • HIPAA
  • IRB submissions
  • Clinicaltrials.gov compliance
  • Human subjects research compliance
  • Clinical trials best practices and standard operating procedures
  • Physician employment contracts

Contact

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