Tiona Hodge

I am a compliance professional with over five years of experience and a Master of Jurisprudence in Business Law & Compliance. I specialize in medical device regulatory frameworks, including FDA Pre-market Submissions, ISO 13485, and EU MDR, and I focus on enterprise-wide risk mitigation and quality improvement.

My background spans regulatory submissions, high-volume compliance documentation management, and implementation of change control and quality assurance protocols across federal and private sectors. I have a proven record of improving documentation efficiency, maintaining 100% adherence to applicable standards, and supporting leadership with investigative reports and regulatory summaries.

I bring practical experience from roles in education, federal contract compliance, legal records review, and legal analysis, and I prioritize clear stakeholder communication, data-driven process improvements, and strict regulatory alignment to reduce risk and ensure operational compliance.