FDA Investigator Diane M Gubernot
Diane M Gubernot has conducted inspections on 17 sites in 3 countries as of 13 Nov 2000. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
17
Last Inspection Date:
13 Nov 2000
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America,
Canada,
Germany
FDA Investigators that have inspected at least one site in common with Diane M Gubernot:
Amy Wyan Mai,
Ana S Cabrera,
Anthony N Onianwa,
Byungja E Marciante,
Christina N Maurino,
Dennis R Hock,
Emily A Walters,
Helen B Ricalde,
Jeffrey A Sincek,
Jennifer A Bazergui,
Jennifer L Custodio,
Jennifer Macmillan,
Justine Tomasso,
Kelly I Anderson,
Kish Bolden,
LCDR Wilfred A Darang,
Li Li,
Lisa Harlan,
Marea K Harmon,
Nerizza B Guerin,
Nikisha M Bolden,
Sarah Forney,
Sinai I Davis,
Tara G Bizjak,
Tara R Gooen,
Thomas E Friel,
Valerie C Reed
Diane M Gubernot's Documents
Publish Date | Document Type | Title |
---|---|---|
August, 2000 | FDA 483 | National Home Products Limited - Form 483, 2000-08-29 |
August, 2000 | EIR | National Home Products Limited - EIR, 2000-08-29 |
April, 2000 | EIR | Bergen Comm Reg Blood Center - EIR, 2000-04-17 |
April, 2000 | FDA 483 | Bergen Comm Reg Blood Center - Form 483, 2000-04-17 |
April, 2000 | FDA 483 Response | Bergen Comm Reg Blood Center - Form 483R, 2000-06-20 |
November, 2000 | FDA 483 | Bergen Comm Reg Blood Center - Form 483, 2000-11-29 |
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