FDA Investigator Sereen Gmorgan Murray
Sereen Gmorgan Murray has conducted inspections on 71 sites in 4 countries as of 18 Oct 2021. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
71
Last Inspection Date:
18 Oct 2021
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
United States of America,
Hungary,
Korea (Republic of),
New Zealand
FDA Investigators that have inspected at least one site in common with Sereen Gmorgan Murray:
Alan R Moore,
Ann B Borromeo,
Anne E Johnson,
Anthony S Puckett,
April R Bowen,
Arlyss M Jones,
Barbara M Frazier,
Betsy C Galliher,
Bonita S Chester,
Brandy D Brown,
Cheryl A Grandinetti,
Christopher M Jeffers,
Claudele S Razo,
Craig A Garmendia,
Cynthia F Kleppinger, MD,
David T Glover,
Dawn C Olenjack,
Derek C Price,
Devaughn Edwards,
Dr. Koffi A Amegadje,
Edward Deberry,
Eileen J Bannerman,
Ernest H Blackwood,
Ingrid A Zambrana,
Jackie M Douglas,
Jawaid Hamid,
John D Lloyd,
Joseph F Owens,
Karen M Cooper,
Kassa Ayalew, MD,
Kent A Conforti,
Lareese K Thomas,
Laura L Staples,
Lawrence Thomas,
Leah M Andrews,
Leon L Crawley,
Marshall A Naimo,
Matthew R Coleman,
Michelle D Haamid,
Michelle M Noe Varga,
Myla D Chapman,
N'jere English,
Nicole M Bell,
Patricia S Smith,
Sandra I Gaul,
Sheri S Oliver,
Stephanie E Hubbard,
Tracy R Ball,
Tyrico K English,
Vanessa E Coulter,
Viviana Matta,
William P Tonkins
Sereen Gmorgan Murray's Documents
Publish Date | Document Type | Title |
---|---|---|
April, 2016 | FDA 483 | J. David Lentz III, M.D. - Form 483, 2016-04-25 |
October, 2019 | FDA 483 | Kennedy, Philip R. - Form 483, 2019-10-16 |
August, 2016 | EIR | Martin Throne MD - EIR, 2016-08-05 |
March, 2016 | EIR | Phoebe Putney Mem Hosp Irc - EIR, 2016-03-03 |
November, 2017 | FDA 483 | O'Barr, Thomas MD - Form 483, 2017-11-30 |
October, 2018 | FDA 483 | Naomi Akita, MD - Form 483, 2018-10-11 |
October, 2016 | EIR | Sagar Lonial, M.D. - EIR, 2016-10-28 |
November, 2021 | FDA 483 | Daniel C. Tarquinio, DO - Form 483, 2021-11-05 |
May, 2021 | EIR | PPD, Inc., part of Thermo Fisher Scientific - EIR, 2021-05-21 |
September, 2019 | FDA 483 | Laura Mulloy, D.O. - Form 483, 2019-09-11 |
February, 2018 | FDA 483 | Wellstar Atlanta Medical Center IRB#1 - Form 483, 2018-02-15 |
March, 2017 | FDA 483 | Robert Donald Harvey - Form 483, 2017-03-24 |
April, 2018 | FDA 483 | Theresa Lawrence Ford - Form 483, 2018-04-03 |
March, 2018 | FDA 483 | Georgia STE DEPT Human Resources IRB#1 - Form 483, 2018-03-08 |
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