Suppliers / Beiersdorf

Beiersdorf

Germany 2 duplicate records merged Updated 9 July 2026

Beiersdorf is a finished-dose manufacturer based in Germany. It appears in 76 regulatory filings across 11 regulators, without an active US DMF or CEP on file. Its filings concentrate with Health Canada, DIGEMAPS (DO) and EMA. Its GMP standing is certified by BPOM (ID), ZLG (DE) and EMA. Its most recent recorded inspection, by US FDA, closed on 9 December 2021 as VAI.

0
active US DMFs
0
valid CEPs
6
registered plants 2 with an FDA FEI number
76
filings across 11 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
2 of 2 confirmed
Inspections
1 of 1 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Inspection history

  • 9 December 2021 VAI US FDA

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

Registered plants

Site FDA FEI
Hamburg, Germany Not on file
Germany, Germany 3002806448
INDEPENDENCIA, Peru Not on file
CABANILLAS DEL CAMPO, Portugal Not on file
Terrugem, Portugal Not on file
Stamford, United States 3010063830

Filings and GMP by regulator

Regulator Filings GMP certificates
Health Canada 32 None
DIGEMAPS (DO) 14 None
EMA 10 2
ISP (CL) 6 None
EEC_EAEU 5 None
DMP (NO) 2 None
BPOM (ID) None 4
ZLG (DE) None 4

Questions about Beiersdorf

Does Beiersdorf hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Beiersdorf. It does have 76 filings with 11 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Beiersdorf FDA-registered?
2 sites operated by Beiersdorf carry an FDA establishment identifier (FEI), which means they are registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Beiersdorf's last inspection go?
The most recent inspection on record closed on 9 December 2021 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 1 inspection is on file.
Where does Beiersdorf manufacture?
6 registered sites are on record, in Germany, Peru, Portugal and United States (Hamburg, Germany and Independencia among others). Every site is listed on this page with the register it came from.
Which regulators recognise Beiersdorf's GMP?
Current GMP certificates are on record from BPOM (ID), ZLG (DE) and EMA. 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 9 December 2021.

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Sources on this page

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