Suppliers / Gp Pharm S.A.U

Gp Pharm S.A.U

Spain Updated 9 July 2026

The public registers hold a second record for Gp Pharm S.A.U. The fuller profile, with 0 active US DMFs and 0 valid CEPs, is at Gp Pharm. Figures on this page cover only this record.

Gp Pharm S.A.U is a contract manufacturer based in Spain. Its GMP standing is certified by US FDA. Its most recent recorded inspection, by US FDA, closed on 21 September 2023 as VAI.

0
active US DMFs
0
valid CEPs
1
registered plants 1 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
3 of 3 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 21 September 2023 VAI US FDA
  • 2 October 2020 VAI US FDA
  • 27 January 2015 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Spain, Spain 3008345811

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA None 1

Questions about Gp Pharm S.A.U

Is Gp Pharm S.A.U FDA-registered?
One site operated by Gp Pharm S.A.U carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Gp Pharm S.A.U's last inspection go?
The most recent inspection on record closed on 21 September 2023 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 3 inspections are on file.
Where does Gp Pharm S.A.U manufacture?
1 registered site is on record, in Spain (Spain). Every site is listed on this page with the register it came from.
Which regulators recognise Gp Pharm S.A.U's GMP?
Current GMP certificates are on record from US FDA. GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Open risk flags

  • The most recent inspection outcome was VAI, on 21 September 2023.

Comparable suppliers

Alcaliber S A also in Spain Altan Pharmaceuticals also in Spain Berlimed also in Spain Casen Recordati, S.L also in Spain Cyndea Pharma, S.L also in Spain

Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates