Attention www.globalkeysolutions.net is now www.keypedia.com, read the full press release here.
KeyPedia LogoKeyPedia Icon
  1. Home
  2. /
  3. Records
  4. /
  5. 483
  6. /
  7. Eric T. Rush M.D
483
•Eric T. Rush M.D•October 24, 2025

FDA 483 - Eric T. Rush M.D - October 24, 2025

View on Dashboard

Your cart

Your cart is empty.

Browse public document pages and click Buy this document. We'll ask for your email at checkout, no account needed up front.

Browse documents

Discuss this record with AI

ChatGPT

Claude

Perplexity

Grok

Copilot

Record Details

An FDA inspection of Eric T. Rush M.D. in Kansas City, MO, revealed significant deficiencies in the conduct of clinical trials. Observations included failure to follow investigational plans, such as missed study visits, unperformed study activities, delayed reporting of serious adverse events, and inadequate documentation of adverse events. Additionally, the firm experienced a lapse in IRB approval for a clinical study due to untimely submission of required documentation.

Company
Eric T. Rush M.D
Inspection Date
October 24, 2025
Product Type
Drugs
Office
Kansas City District Office
Person
  • Logan M. Jones
Open in Dashboard

ID · a727092f-e804-4b8e-9adf-c5a5cf2b747a

footer
Global Key Solutions
Regulatory Data Transformed
Contact
New York Office:
370 Jay Street 7th Floor
Brooklyn, NY 11201
Scranton Office:
Scranton Enterprise Center, Suite 217
201 Lackawanna Avenue
Scranton, PA, 18503
🇺🇸+1 917-789-5099
🇪🇺+48 532-447-507
info@globalkeysolutions.net
Quick Links
HomePlatform OverviewMedia
KeyPedia™ Lite
Browse HubDatabase DirectoryRecordsCompaniesOfficesPeopleCareersAbout UsFounding TeamMeet Our ExpertsPartners
Legal & Ethics
Privacy PolicyTerms of ServiceOur Values & MissionCode of Ethics & AI Policy
©2026, Global Key Solutions All rights reserved.