I am the Vice President of Marketing for all Business Units at Global Regulatory Writing & Consulting. In this role I develop strategy and work with subject matter experts to plan and execute marketing campaigns.Previously I was the senior director for the medical device team at Global Regulatory Writing & Consulting. I led a large team of regulatory writers and consultants with a primary focus on Clinical Evaluations under EU MDR. This team has written many hundreds of CERs since 2015 for our clients and has broad experience working in multiple therapeutic areas.Before working at Global I was a litigator with a focus on family law, civil cases, and probate. After several years of practice I started my own law firm and then entered the field of medical writing.