FDA Investigator Linda Kuchanthal
Linda Kuchanthal has inspections in 1 countries as of 04 Mar 2022. Linda Kuchanthal has collaborated with a combined 554 experts on various inspections, contributing to compliance and improvement across diverse sectors.
Investigator Details
Number of Inspected Sites:
1
Last Inspection Date:
04 Mar 2022
Investigator Role:
FDA Investigation Participant
Redica ID:
Country:
United States of America
Co-Investigator(s):
Alan E Mehl,
Brittany D Terhar,
Carl J Montgomery,
Chilton L Ng,
Chris A Sack,
Danial S Hutchison,
Daniel R Hurt,
Dr. Sriram Subramaniam, PhD,
Evelyne L Weaver,
Farhana Khan,
Gretchen Lf Trendel,
Gwyn G Dickinson,
Ingrid Y Johnson,
Jill J Tillman,
Julie N Vosilus,
Kellia N Hicks,
Linda R Kuchenthal,
Martin K Yau, PhD,
Matthew R Sleeter,
Michael S Smoker,
Michele L Obert,
Monique M Brooks,
Neal L Adams,
Rita K Kabaso,
Shirley J Berryman,
Shwnji Susie Lee,
Susie H Lee,
Tara L Greene,
Victoria A Wagoner,
Vinh T Phan,
Wayne D Mcgrath,
Zachary A Bogorad
Linda Kuchanthal's Documents
Publish Date | Document Type | Title |
---|---|---|
August, 2004 | FDA 483 Response | Catalent CTS, LLC - Form 483R, 2004-08-30 |
August, 2004 | FDA 483 | Catalent CTS, LLC - Form 483, 2004-08-20 |
August, 2004 | EIR | Catalent CTS, LLC - EIR, 2004-08-20 |
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