Sandra Reid
Specialist
O: 651.412.8601
M: 951.858.0327
Sandra Reid specializes in consulting with medical technology and pharmaceutical companies on FDA matters, including pharmaceutical labeling, and regulatory questions. She is skilled in U.S. Food and Drug Administration (FDA), Medical Devices and Life Sciences industries.
Representative Experience
• Ad promo review
• OPDP Advisory Submissions including DTC campaigns
• Labeling Review
• Experience with FDA submissions (NDA, IND, IDE, De Novo)
• Compliance
• Manufacturing
• GMP/cGMP
Education
• 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)
Bar Admissions and Qualifications
• Regulatory Affairs Certified (RAC) through the Regulatory Affairs Program at California State University, East Bay (Hayward, California)
Memberships
• Member of the Regulatory Affairs Professionals Society (RAPS)