FDA 483 OBSERVATION · #1194 OF 1,932 MOST-CITED

Continuing review

FDA cited this observation 13 times across 13 firms in recent inspections. Below: how it breaks down by program area and fiscal year, and real examples of how FDA worded it on Form FDA 483.

What this grouping is not

An observation-type page groups FDA’s published citation records. The grouping, the compliance steps and the root causes are SPEQ synthesis, not an FDA classification of any citation, and a count measures what FDA published rather than risk.

BY PROGRAM AREA
Bioresearch Monitoring13
BY FISCAL YEAR
FY20241
FY20232
FY20202
FY20193
FY20182
FY20163

How FDA worded it — real examples

The IRB does not conduct continuing review of research at intervals of not less than once per year.

ACMH Hospital IRB · Kittanning, Pennsylvania · Bioresearch Monitoring · 2023-11-08

The IRB does not conduct continuing review of research at intervals of not less than once per year.

Glens Falls Hospital IRB · Glens Falls, New York · Bioresearch Monitoring · 2023-08-14

The IRB does not conduct continuing review of research at intervals of not less than once per year.

Louisiana State University Health Sciences Center IRB · New Orleans, Louisiana · Bioresearch Monitoring · 2023-07-26

The IRB does not conduct continuing review of research at intervals of not less than once per year.

Jackson-Madison County General Hospital IRB · Jackson, Tennessee · Bioresearch Monitoring · 2019-11-26

The IRB does not conduct continuing review of research at intervals of not less than once per year.

Western Reserve Health Education IRB · Youngstown, Ohio · Bioresearch Monitoring · 2019-11-20

The IRB does not conduct continuing review of research at intervals of not less than once per year.

Bellin Health System Inc., IRB · Green Bay, Wisconsin · Bioresearch Monitoring · 2019-05-09

Related SPEQ references

Where to read the requirements behind this observation area on SPEQ. These are SPEQ's topic and audience pages — not an FDA classification of the citation.

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Examples are a representative sample of FDA's published inspection observations. Open the 483 observation explorer →