Prerna Sharma Menon

About Prerna Sharma Menon

Throughout my 15+ year career, I have cultivated a reputation as a results-oriented VP of Regulatory Affairs with a track record of enabling clinical, CMC, and non-clinical development, with experience in both early- and late-stage product development. I am dedicated to building high-performing teams, driving continuous improvement, and ensuring strict regulatory compliance. Some of the competencies and personal attributes that make me a valuable asset to any company include the following: • Talented strategist with a history of creating effective regulatory plans, using a blend of technical and scientific knowledge, business acumen, and insight into the ever-changing regulatory landscape. • Exceptional communicator and relationship builder with the capacity to act as a trusted liaison when dealing with regulatory agencies such as the FDA and EMA. • Influential subject matter expert and invaluable resource to internal teams and the senior executive committee with a history of guiding products from ideation to Proof of Concept. • Able to conduct intensive due diligence on range of potential development opportunities. • Natural problem solver with history of overcoming obstacles by designing innovative solutions.

Experience

1. VP and Head of Regulatory Affairs

   Surrozen

   Dec 2021 — Present · South San Francisco, CA, US

Education

• Institute of Chemical Technology (formerly called UDCT), Mumbai, India

  BS

• University of Oklahoma, College of Pharmacy

  Ph.D.