FDA Investigator Kelly J Pegg
Kelly J Pegg has inspections in 1 countries as of 26 Feb 2019. Kelly J Pegg has collaborated with a combined 318 experts on various inspections, contributing to compliance and improvement across diverse sectors.
Investigator Details
Number of Inspected Sites:
18
Last Inspection Date:
26 Feb 2019
Investigator Role:
FDA Investigator
Redica ID:
Country:
United States of America
Co-Investigator(s):
Anya D Lockett Evans,
Brenda G Stewart Munoz,
Brenda Stewart Munoz,
Camille D Brown,
Charles D Brown,
Christopher D Rush,
Christopher J Smith,
Cynthia A Harris, MD, RN,
Elisa M Fleming,
Elizabeth A Waltrip,
Leighton K Ngai,
Phillip D Waldron,
Rhonda L Dash,
Ronda R Loyd Jones,
Travis M Beard,
Ve Garcia,
Vivian Garcia
Kelly J Pegg's Documents
Publish Date | Document Type | Title |
---|---|---|
August, 2001 | EIR | John E Pippen, MD - EIR, 2001-08-27 |
January, 2002 | EIR | Alan Menter, MD/Clin Inv - EIR, 2002-01-18 |
May, 2001 | FDA 483 | Urology Clinics of North Texas - Form 483, 2001-05-03 |
December, 2000 | EIR | Henry A Punzi, MD - EIR, 2000-12-18 |
February, 2000 | EIR | Roy M. Fleischmann, M.D. - EIR, 2000-03-17 |
July, 2001 | EIR | Nicholaos C Bellos, MD - EIR, 2001-07-18 |
November, 2001 | EIR | Southwest Independent Irb - EIR, 2001-11-19 |
February, 2000 | FDA 483 Response | Roy M. Fleischmann, M.D. - Form 483R, 2000-02-09 |
May, 2001 | EIR | Brian A Feagins, MD - EIR, 2001-05-03 |
January, 2002 | FDA 483 | Alan Menter, MD/Clin Inv - Form 483, 2002-01-18 |
February, 2000 | FDA 483 | Roy M. Fleischmann, M.D. - Form 483, 2000-02-02 |
August, 2001 | FDA 483 | John E Pippen, MD - Form 483, 2001-08-29 |
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](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