C. R. Bard
Covington, GA
Works in Cardiovascular · Genetic & rare · GI & liver · Neurology · Oncology · Psychiatry · Renal & urogenital · Respiratory · Women's health
C. R. Bard is a clinical trial sponsor based in Covington, GA. It has 10 active clinical trials with 2,588 planned participants, across 9 therapeutic areas. Since 2021 it has completed 38 trials and stopped 5 early. Its FDA record on file shows 1 inspection and 6 recalls.
Trial track record · since 2021
FDA record
Recent FDA actions
Pipeline · 10 active trials
| Stage | Trial | Status |
|---|---|---|
Questions about C. R. Bard
No warning letter naming C. R. Bard is on file. FDA has published 1 inspection classification and 6 recalls naming it.
FDA has posted 1 inspection classification naming C. R. Bard. The latest inspection ended on 2026-06-05 and was classified VAI (voluntary action indicated). FDA posts a classification after its review, often months after the inspection ended.
Yes. FDA's enforcement reports list 6 recalls by C. R. Bard; the latest, reported on 2026-09-16, is a Class II recall.
C. R. Bard is lead sponsor of 10 active clinical trials on ClinicalTrials.gov, with 2,588 planned participants, in Cardiovascular, Genetic & rare, GI & liver, Neurology and other areas. Since 2021 it has completed 38 trials and stopped 5 early.
C. R. Bard is based in Covington, GA. The address is the one on its FDA records or ClinicalTrials.gov registrations, which name the establishment or the registrant, not always the group's head office.
From public sources only: ClinicalTrials.gov for trials, FDA's Data Dashboard, warning-letter listing and enforcement reports for the FDA record, and SEC filings for financials. Approve Suite is not affiliated with C. R. Bard; every record links to the source, and nothing here is advice.
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Trial counts are as the sponsor reported them to ClinicalTrials.gov, for trials changed since 2021; latest update 2026-10-02.
The FDA record counts inspection classifications, warning letters and recalls FDA has published that name this company. Compare it with the industry in the free CDMO FDA inspection lookup.
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