Sandra Reid, J.D., R.A.C., Consultant

sreid@gardner.law
‭+1 (651) 412-8601 office
‭+1 (951) 858-0327 mobile

Sandra Reid specializes in consulting with medical technology and pharmaceutical companies on FDA matters, including pharmaceutical labeling, and regulatory questions. Prior to practicing at Gardner Law, she worked in various management roles at XenoPort, Allergan, Dey Laboratories and Genentech. Sandra is an active member in My Life My Mentor youth program and her church.

18+


YEARS OF EXPERIENCE IN THE PHARMACEUTICAL INDUSTRY

3


GENERATIONS OF SANDRA'S IN HER IMMEDIATE FAMILY

"Don't forget to do good and to share with those in need." Hebrews 13:16. My passion for working in the pharmaceutical/biotechnology/medical device industries comes from love and desire to help others in need.
– Sandra Reid, J.D., R.A.C.
Practice areas:
  • Advertising and Promotional Compliance Review
  • OPDP Advisory Submissions including DTC campaigns
  • Compliance Assessments
  • Labeling Review
  • NDA
  • IND
  • IDE
  • De Novo
  • Manufacturing
  • GMP/cGMP

Prior to Gardner Law Sandra worked in the pharmaceutical industry for 18 years at Genentech, Dey Laboratories, Allergan and XenoPort, prior to becoming an owner and Principal Consultant at S. R. Reid Consulting Services, Inc.

  • Member of the Regulatory Affairs Professionals Society (RAPS)
  • Active member of Faith Landmark Missionary Baptist Church
  • Mentor in My Life My Mentor youth mentor-ship program
  • Juris Doctor, Trinity International University (Deerfield, Illinois)
  • Master of Arts, Leadership, Saint Mary’s College of California (Morago, California)
  • Bachelor of Science, Biology, University of California, Riverside (Riverside, California)
  • Regulatory Affairs Certified (RAC) through the Regulatory Affairs Program at California State University, East Bay (Hayward, California)
  • Regulatory Affairs Certified (RAC) through the Regulatory Affairs Professionals Society (RAPS)