FDA Investigator Lauren N Barber
Lauren N Barber has conducted inspections on 8 sites in 1 countries as of 17 Mar 2022. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
8
Last Inspection Date:
17 Mar 2022
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America
FDA Investigators that have inspected at least one site in common with Lauren N Barber:
Amber G Wardwell,
Andrew J Howard,
Anita R Michael,
Annet R Rajan,
Anthony W Hite,
Chaltu Nwakijra,
Clarice J Ahn,
Cynthia A Harris, MD, RN,
Daniel L Zheng,
David A Oluwo,
David P Rice, Jr,
Denise R Beuttenmuller,
Donald C Obenhuber, PhD,
Dr. Zhihao Qiu (Peter), PhD,
Edward P Potter,
Emest F Bizjak,
Eric L Dong, BS,
Esaw,
Graeme E Price,
Graeme Price,
Helen Verdel,
Jaison J Eapen,
Jamie D Swann,
Jennie A Eng,
Jessica K Yoon,
Joanne M Hajoway,
John Dan,
John P Mistler,
Jonathan W Chapman,
Julie M Anbarchian,
Junho Pak,
Karen A Spencer,
Kathleen M Jordan,
Kenneth Nieves,
Laurie B Frazier,
Lori A Holmquist,
Lori M Newman,
Megan A Haggerty,
Michael Shanks, MS,
Michele M Falchek,
Mohamad A Chahine,
Monica Commerford, PhD,
Nancy L Meade,
Nina D Patel,
Nirjal Bhattarai,
Osama M Hamoud,
Patricia F Hughes, PhD,
Paul L Bellamy,
Rachel C Harrington,
Rina Bhikha,
Robert J Martin,
Sean R Marcsisin,
Seemay A Lee,
Sherry L Secrist, BLT DO,
Stephen J Koniers,
Suzanne M Healy,
Tammy L Chavis,
Tania E Vizcaino,
Teresa L Fox,
Thuy T Nguyen, LCDR,
Toyin B Oladimeji,
Viviana R Ramirez,
Walter L Fava,
Wayne L Jefferson,
William D Murray,
Zhongren Wu
Lauren N Barber's Documents
Publish Date | Document Type | Title |
---|---|---|
March, 2022 | FDA 483 | ImmuCell Corporation - Form 483, 2022-03-29 |
September, 2021 | FDA 483 | W.S. BADGER COMPANY, INC. - Form 483, 2021-09-14 |
November, 2021 | FDA 483 | Micron Inc - Form 483, 2021-11-05 |
January, 2020 | FDA 483 | Bristol-Myers Squibb Company - Form 483, 2020-01-10 |
November, 2021 | EIR | Micron Inc - EIR, 2021-11-05 |
Experience Redica Systems’ NEW investigator profiles and dashboards
Redica Systems customers get access to over 1,400 FDA Investigator profiles, containing powerful analysis like:
- Total inspections conducted
- 483 rate
- OAI rate
- Warning Letter rate
- Inspections by Industry, Scope, and Inspection Reason
- And much more
Investigator Profiles are not sold as on-demand documents. If you’d like to see one, fill out the form below to connect with our Sales Team and get it in your inbox as little as 24 hours.
![FDA Investigator Profile Icon](/images/InspectorProfile.png)
Talk to sales to access our investigator profiles
Loading...
Investigator Profiles Are Just the Tip of the Iceberg
Becoming a Redica Systems customer not only provides you with unlimited access to profiles similar to the one above for every current and former FDA Investigator, but also grants you access to:
Inspection Intelligence
- Pre-Approval Inspection (PAI) trends
- The ability to filter nearly any FDA enforcement action by GxP labels like GMP, GCP, etc.
- Latest 483s: see what the trends are across all FDA Investigators
- CFR Heatmap: Citations aggregated by Subpart by Year
Vendor Intelligence
- Full inspection histories for your vendors down to the specific site level
- All of the functionality mentioned above but isolated to just your vendors
Regulatory Intelligence
- Zero in on the trends for a specific agency/regulator (ex. FDA, MHRA, EMA, Health Canada)
- All the latest "Signals" from agencies around the world, segmented by Country, Type (ex. Guidance, Decree...), Category (ex. Rules/Regulations/Guidance, News, Reports...), Theme (ex. Cell and Gene Therapy, AI...), and more