FDA Investigator Krishna Ghosh, PhD
Krishna Ghosh, PhD has conducted inspections on 12 sites in 7 countries as of 21 Mar 2024. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
12
Last Inspection Date:
21 Mar 2024
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America,
Puerto Rico,
Netherlands,
Belgium,
Italy,
India,
China
FDA Investigators that have inspected at least one site in common with Krishna Ghosh, PhD:
Angela E Glenn,
Ariel Cruz Figueroa,
Arlene M Badillo,
Bapu R Gaddam,
Barbara Janine Breithaupt,
Brenda W Uratani, PhD,
Brian D Nicholson,
Carrie A Hughes,
Christopher T Middendorf,
Daniel L Obrzut,
Dr. Gang Wang, PhD,
Edwin Martinez,
Gary J Lehr,
German Rivera,
Jacob G Lutz,
Jeffrey D Meng,
Jorge L Guadalupe,
Jose A Lopez,
José E Meléndez,
Junho Pak,
Kenneth H Williams,
Kham Phommachanh,
Lareese K Thomas,
Laurimer Kuilan Torres,
Libia M Lugo,
Lori B Wikstrom,
Marian E Ramirez,
Marianela Aponte Cruz,
Matthew M Schuckmann,
Michele Perry Williams,
Mindy M Chou,
Myriam M Sosa,
Noreen Muñiz,
Parul M Patel,
Patrick C Klotzbuecher,
Paul Mouris,
Ramon A Hernandez,
Rapti D Madurawe,
Raquel Gonzalez Rivera,
Rebecca Parrilla,
Robert C Steyert,
Robert D Tollefsen,
Robert J Ham,
Roger F Zabinski,
Ross J Grigsby,
Sony Mathews,
Susanna E Ford,
Tracey L Harris,
Uttaniti Limchumroon (Tom),
Valentino Fiorella,
Vilmary Negron Rodriguez,
Vioela J Caze,
Xiaokuang Lai, PhD,
Yifan Wang,
Ying Zhang
Krishna Ghosh, PhD's Documents
Publish Date | Document Type | Title |
---|---|---|
January, 2020 | FDA 483 | PETNET SOLUTIONS, INC. - Form 483, 2020-01-31 |
August, 2016 | FDA 483 | Advanced Accelerator Applications (Italy) SRL - Form 483, 2016-08-12 |
January, 2020 | FDA 483 Response | PETNET SOLUTIONS, INC. - Form 483R, 2020-02-20 |
July, 2013 | FDA 483 | University of Washington PET Radiochemistry Laboratory - Form 483, 2013-07-18 |
January, 2020 | EIR | PETNET SOLUTIONS, INC. - EIR, 2020-01-31 |
August, 2015 | FDA 483 | Unimark Remedies Limited - Form 483, 2015-08-14 |
July, 2017 | FDA 483 | Lilly del Caribe, Inc. - Form 483, 2017-07-21 |
July, 2019 | FDA 483 | Lilly del Caribe, Inc. - Form 483, 2019-07-12 |
May, 2013 | FDA 483 | The Feinstein Institutes for Medical Research - Form 483, 2013-05-09 |
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](https://redica.com/document-store/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