Vivian Lauderdale

Vivian brings over 25 years of experience from the biotechnology industry with expertise in regulatory affairs, cGMP quality systems, and biomedical business management. She has strong grant writing expertise and has successfully obtained awards from the SBIR, NIH, DoD, and NSF. She also holds a Regulatory Affairs Certification (RAC) from the US Regulatory Affairs Professional Society (RAPS). Vivian holds an MS from George Washington University Medical School Division and an Executive MBA from UCLA.