Biography

I am a graduate of Northeastern’s Master’s in Regulatory Affairs for Drugs, Biologics, and Medical Devices online program.  I am currently a pre-approval manager – regulatory affairs at a pharmaceutical company that develops veterinary drug products. My background in FDA-regulated businesses includes regulatory affairs, regulatory compliance, quality control microbiology, quality assurance, and validation.   I have bachelor’s degrees in both biology and chemistry from West Virginia Wesleyan College and a juris doctor from Texas Wesleyan University School of Law.  I am licensed to practice law in the state of Texas.

Professional Experience

Huvepharma, Inc.    

  • Pre-Approval Manager – Regulatory Affairs – Large animal pharmaceuticals – medicated feeds and food additives – enzymes

Virbac Corporation  

  • Senior Manager, Regulatory Affairs – Companion animal pharmaceuticals, feeds

Neos Therapeutics   

  • Regulatory Affairs Manager Human pharmaceuticals – generics, 505(b)(2) new drugs, OTC, and dietary supplements

Cardinal Health Quality Assurance

  • Engineer and Validation Specialist – human pharmaceuticals

Professional Activities & Accomplishments

State Bar of Texas member

Generic Animal Drug Association member

Education

JD from Wesleyan University (2002)

Area of Expertise

FDA and USDA Regulatory, Promotion and Advertising of FDA Regulated products, Regulatory Affairs, Regulatory Compliance, veterinary pharmaceutical regulatory affairs