Sherry Parker, PhD

Office Hours with Sherry Parker, PhD, WuXi AppTec

Technical & Regulatory Expert - March 1st

Our office hours are hosted by leading experts who have generously offered their services pro bono to our entrepreneurs. 

To hold your slot for this session, we require a $100 credit card deposit. The deposit will be refunded the day after you attend. No-shows will not receive a refund. Please be punctual; arrivals late by more than 15 minutes will be considered no-shows.

To Sign Up:

  1. Select your time slot below and fill in the information
  2. Make the refundable* deposit payment below or by clicking here
  3. You are done!

*Please note that you may request a refund up to 48 hours in advance. (This will give us time to offer the time slot to the first person on the waitlist.) We regret that we cannot honor requests made at a later time.

Waitlist

If all scheduled slots are full, please sign up for a waitlist slot. If an opening appears, we will contact people in the order they signed up. Waitlist time slots will be confirmed 48 hours prior to office hours. Deposit payment will be required upon time slot confirmation.

Location

Byers Hall, Suite 214, UCSF Mission Bay
1700 4th St, San Francisco, CA 94158

About Sherry Parker:

parker website.jpg

Dr. Parker has over 19 years of toxicology and medical device research experience, and is an expert in analytical, pharmacological, and toxicological evaluations of devices and novel combination products. After receiving her Ph.D. in Molecular and Cellular Pharmacology from the University of Miami, Dr. Parker spent 10 years in toxicology research for the University of Miami, the U.S. EPA (Neurotoxicology Division) and RTI International before moving into the medical device industry, where for more than six years she was involved with device development, safety and efficacy testing and regulatory submissions for OrbusNeich Medical. In her current position as WuXi AppTec’s Director of Technical and Regulatory for Medical Devices/ Combination Products, Dr. Parker provides manufacturers with guidance on global regulatory and technical requirements and testing program design. Dr. Parker is currently an internationally recognized expert by ISO and US Delegate for TC 194, the technical committee for ISO 10993. She is currently the Vice President-Elect for the Medical Device and Combination Products Specialty Section of the Society of Toxicology.