FDA Investigator Sarah Ibrahim
Sarah Ibrahim has conducted inspections on 2 sites in 2 countries as of 27 Aug 2018. See below for a list of the FDA enforcement documents resulting from those inspections.
Investigator Details
Number of Inspected Sites:
2
Last Inspection Date:
27 Aug 2018
Investigator Role:
FDA Investigator
Redica ID:
Countries of Inspections:
India,
United States of America
FDA Investigators that have inspected at least one site in common with Sarah Ibrahim:
Angela E Glenn,
Azza Talaat,
Barbara Janine Breithaupt,
Caroline Strasinger,
CDR Ileana Barreto Pettit,
Cheryl A Clausen,
Daniel J Roberts,
Dongping Dai, PhD,
Farhana Khan,
Jeffery A Hangartner,
Jennifer Lalama,
Jennifer M Menendez,
Jessica L Pressley,
José E Meléndez,
Jose M Cayuela,
Jose Martinez, Jr,
Katherine Szestypalow,
Kayla V Sprague,
Kejun Cheng,
Kellia N Hicks,
Lillian Mcolon Mcknight,
LT Richard A Lyght,
Monica Cburgos Garcia,
Muralidhara B Gavini, PhD,
Noreen Muñiz,
Parul M Patel,
Patrick C Klotzbuecher,
Rebecca E Dombrowski,
Robert C Coleman,
Roy R Rinc,
Saleem A Akhtar,
Santos E Camara,
Sarah E Mcmullen,
Scott B Laufenberg,
Scott T Ballard,
Simone E Pitts,
Thomas J Arista,
Victor Spanioli,
Vilmary Negron Rodriguez,
Walden H Lee
Sarah Ibrahim's Documents
Publish Date | Document Type | Title |
---|---|---|
July, 2015 | FDA 483 | Noven Pharmaceuticals, Inc. - Form 483, 2015-07-10 |
August, 2018 | FDA 483 | Sun Pharmaceutical Industries Limited - Form 483, 2018-08-31 |
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