Ravis Radley
FDA investigator
Appears on 1 document from 2024, mostly at sites in Italy. Most often cites general requirements (21 CFR 211.160(a)).
- 1
- Documents on file
- 5.0
- Observations per 483
- 2024
- First seen
- 2024
- Most recent
What they cite most
From 5 observations- 21 CFR 211.160(a)General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
- 21 CFR 211.25(a)Personnel qualifications1
- 21 CFR 314.80(c)(1)(i)Postmarketing reporting of adverse drug experiences1
Activity by year
2024: 1
Where
Italy 1
Often inspects with
Is Ravis Radley coming to your site?
Our team writes custom reports before an inspection: what this investigator cites most, how they write it up, and how your site's history compares, in one brief you can circulate.
Ask about any investigator in Claude or ChatGPT with the AI connector.
Inspection history
1 document, newest first| Date | Firm | Location | Observations | Open |
|---|---|---|---|---|
| 2024-01-26 | 483 GlaxoSmithKline Vaccines SrlJan 26, 2024 · Sovicille, Italy | Sovicille, Italy | 5 |
About this profile
What does Ravis Radley inspect?
Ravis Radley appears on 1 document on file covering 1 site, mostly in Italy.
What do they cite most often?
21 CFR 211.160(a) (general requirements), followed by 21 CFR 211.192 and 21 CFR 211.22(d).
Can I read the observations?
Each document page previews the opening words of every observation. The full documents are available to buy, one at a time or together.
How current is this profile?
The most recent document on file for Ravis Radley is dated Jan 26, 2024.