FDA Clinical Investigator Disqualification List

Review available FDA clinical investigator disqualification records and source status. Distinguish disqualified, restricted and reinstated investigators.

Source availability

Available for screening

232 source records are available in the current dataset.

Records can overlap across lists; this is not a count of unique people or organizations.

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Dataset statistics

Data overview

Statistics checked

FDA Clinical Investigator Disqualification Proceedings is published by United States Food and Drug Administration.

The available version contains 232 source records before any name search.

The entity-type breakdown is 232 people.

Source records
232
Publicly browsable records
232
Entity types present
1
Record types and how to read these counts

Records by entity type

Other / unspecified
0

What these numbers mean

Counts describe this source’s current available records, before any name search. Records can overlap within and across lists. They are not counts of unique entities.

Publicly browsable records are the portion available in the public directory. A record’s presence does not by itself establish an active sanction.

Organizations include companies and other bodies. Other / unspecified means the source record has no more specific supported type.

What this source covers

The complete FDA table includes disqualified investigators, restricted agreements, reinstated investigators, removed restrictions and proceedings that did not result in disqualification. It is not an inspection-results database, a financial sanctions list or a list of people uniformly banned from clinical work.

Distinguish the action from its current effect

Compare the official FDA record ID and the current status. Totally Restricted is FDA’s historical wording for disqualification; Restricted means the investigator remains eligible subject to an agreement. Reinstated, restrictions-removed, not-disqualified and adequate-assurance records are retained as history and excluded from current restriction matching. Original proceedings and status dates remain distinct; no legal start or end date is invented.

  • Read the stated action type and procedural status.
  • Check the decision, dates and later amendments.
  • Keep different orders about the same named party distinct.

FDA Clinical Investigator Disqualification Proceedings records

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Questions about US FDA Clinical Investigator Disqualification Proceedings

Does an FDA investigator listing mean the person is disqualified?

No. Read FDA's stated status and the linked case documents. The database covers past and current proceedings. It includes people who were disqualified, people working under a restricted agreement, people later reinstated, and cases that did not lead to a ban. These outcomes are not the same. A restricted investigator may still receive investigational products if the agreement allows it. FDA's old phrase “totally restricted” means disqualified, rather than the less severe restricted status. “Restrictions removed” means the agreement's limits no longer apply. Check that the entry concerns the person you mean and that its status still applies. An old case alone does not prove a current ban. This database is separate from the FDA drug-product debarment list. Read the publisher’s FDA Clinical Investigator Disqualification Proceedings guidance.

Who publishes US FDA Clinical Investigator Disqualification Proceedings?

The catalog identifies US Food and Drug Administration as the publisher in United States. Open the publisher reference. SanctionsKit’s source profile is separate from that publisher’s original records and notices.

Can I select US FDA Clinical Investigator Disqualification Proceedings for screening?

The current source snapshot marks US FDA Clinical Investigator Disqualification Proceedings as available for screening. Select its source ID, us-fda-restricted, when your policy requires it. Check availability again when you run a request. This status does not by itself grant public browsing or export rights.

Can I browse current US FDA Clinical Investigator Disqualification Proceedings records here?

Current public records from US FDA Clinical Investigator Disqualification Proceedings can be browsed here. The current source contains 232 records. This counts source records, not distinct people, companies or assets. An empty name search is not a completed screening check.

May I reuse or export US FDA Clinical Investigator Disqualification Proceedings records?

Access to US FDA Clinical Investigator Disqualification Proceedings does not grant every right to copy, export or redistribute it. Read the source reuse terms and the attribution notice for the version you use. A public record page or working screening integration is not an export permission. Follow the conditions that apply to your intended use.

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Source discovery reference: OpenSanctions source catalog, captured . Import and record counts above come from SanctionsKit.