QA Consulting Hires Consultant Gretchen Upton
Seasoned regulatory and quality professional has broad expertise
Austin, Texas - Jan. 10, 2020 – QA Consulting, Inc. has hired Gretchen Upton as a Regulatory and Quality Consultant.
Gretchen specializes in creating and maintaining quality systems and gaining clearance for device applications in various FDA divisions, including orthopedic and software decision support. She also specializes in creating and maintaining CE mark documents.
“We are pleased to have Gretchen join our experienced team of consultants,” says QA Consulting CEO and Founder, Anne Holland. “She brings more than 17 years of experience in medical device development and clinical research trials.”
As a QA/RA/Clinical Research professional, Gretchen has worked with companies such as Menninger Clinic, The Cleveland Clinic, BioMedical Enterprises (DePuy Synthes), and Dascena.
She currently serves on both the Texas Medical Device Alliance (TMDA) committee and FDA Medical Device Industry Coalition (FMDIC).
Gretchen holds a Bachelor’s degree from Kansas State University. Her certifications include Regulatory Affairs Certification (RAC) through the Regulatory Affairs Professional Society (RAPS), Certified Quality Auditor (CQA) from the American Society for Quality (ASQ) and she also is a Certified Clinical Research Professional (CCRP) from the Society of Clinical Research Associates (SOCRA).
About QA Consulting
For 20 years QA Consulting, Inc. has provided comprehensive, personalized consulting services for today’s medical device industry including QMS, auditing, regulatory affairs, and microbiological services. QA Consulting’s staff of expert consultants provide unique and creative solutions, and unparalleled customer service to early stage, midsize, and Fortune 500 medical device companies. Learn more at qaconsultinginc.com.