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
• HIPAA
• IRB submissions
• Clinicaltrials.gov compliance
• Human subjects research compliance
• Clinical trials best practices and standard operating procedures
• Physician employment contracts

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