.png)
.png)
Director, Manufacturing Quality Guidance and Policy Staff, CDER
U.S. FDA
CDR Tara Gooen Bizjak is the Director of the Manufacturing Quality Guidance and Policy Staff in CDER, Office of Compliance, Office of Manufacturing Quality and is an engineering officer in the United States Public Health Service. Tara has been with the FDA for 19 years and has focused in the area of drug manufacturing, current good manufacturing practice (CGMP) inspections, and related policy. She started as a field investigator in the New Jersey District and transferred to CDER in 2007. Prior to her current role, she was a senior science policy advisory in the Office of Pharmaceutical Quality in the area of quality metrics and emerging technology, branch chief in the area of drug manufacturing pre-approval inspections and a senior advisor in the Office of Regulatory Affair’s Office of Policy and Risk Management. CDR Bizjak is an ASQ (American Society for Quality) Certified Quality Engineer and Quality Improvement Associate. She received a B.S. in Chemical Engineering from Cornell University and a Masters in Biomedical Science from Rutgers University.
Monday, September 27, 2021
15:30 – 16:17 EDT
Monday, September 27, 2021
16:17 – 17:00 EDT
Tuesday, September 28, 2021
14:23 – 15:00 EDT
Tuesday, September 28, 2021
16:09 – 16:34 EDT
Tuesday, September 28, 2021
16:34 – 17:00 EDT
Wednesday, September 29, 2021
11:45 – 13:15 EDT
Wednesday, September 29, 2021
12:35 – 13:15 EDT