FDA Investigator Tamara M Qtami
Tamara M Qtami has conducted inspections on 16 sites in 1 countries as of 27 Jan 2016. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
16
Last Inspection Date:
27 Jan 2016
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 Tamara M Qtami:
Adam J Taylor,
Ana L Kewes,
Anthony R Ronga,
Ashley L Reiber,
Audrey Dela Cruz,
Brian P Emanuel,
Brittany R Laymon,
Bruce H Mccullough,
Carol F Robinson,
Charles H Spivey,
Charlie P Booker,
Chase S Baldwin,
Cheryl A Kmiec,
Christopher D Leach,
Clotia Cabbey Mensah,
Dariusz Galezowski,
David J Gasparovich,
Debra I Love,
Debra Lboyd Seale,
Esther A Ofori,
Humera T Khan,
James E Roberts,
Janae D Price,
Jason F Chancey,
Jennifer C Adams,
Jennifer C Johnson,
Joseph D Cooper,
Joshua M Adams,
Kathleen S Tormey,
Laster B Shealey,
Latoya A Griffith,
Lee Terry Moore,
Lequita M Mayhew,
Lisa Hayka,
Marcia A Worley,
Margaret Torres Vazquez,
Mark G Peterson,
Michael D Robinson,
Michael R Giammanco,
Nicole J Clausen,
Pablo Alcantara,
Paola S Barnett,
Patrick E Gainer,
Roberta W Cunningham,
Scott A Krause,
Shalonda C Clifford,
Shana L Williams,
Sullan,
Susan W Ciani,
Tamara Qtami,
Tara C Alcazar,
Thomas W Nojek,
Timothy Brennan,
William D Sherman,
William G Nelson,
William R Weissinger,
Yuriy Solovyov
Tamara M Qtami's Documents
Publish Date | Document Type | Title |
---|---|---|
November, 2015 | FDA 483 | Azazuddin A. Ahmed, MD - Form 483, 2015-11-30 |
December, 2014 | FDA 483 | Sookyong Koh, M.D. - Form 483, 2014-12-19 |
December, 2014 | FDA 483 Response | Sookyong Koh, M.D. - Form 483R, 2015-01-13 |
November, 2015 | EIR | Azazuddin A. Ahmed, MD - EIR, 2015-11-30 |
November, 2015 | FDA 483 Response | Azazuddin A. Ahmed, MD - Form 483R, 2015-12-14 |
December, 2014 | EIR | Sookyong Koh, M.D. - EIR, 2014-12-19 |
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