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

Email     sreid@gardner.law
Office    651.412.8601
Mobile   951.858.0327

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 Experience in the Pharmaceutical Industry

3

Generations of Sandras 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:

  • Ad promo review
  • OPDP Advisory Submissions including DTC campaigns
  • Labeling Review
  • NDA
  • IND
  • IDE
  • De Novo
  • Compliance
  • Manufacturing
  • GMP/cGMP