Ferring

Germany 3 duplicate records merged Updated 9 July 2026

Ferring is a finished-dose manufacturer based in Germany. It appears in 1,215 regulatory filings across 39 regulators, without an active US DMF or CEP on file. Its filings concentrate with Health Canada, MHRA (UK) and EMA. Its GMP standing is certified by ZLG (DE), BPOM (ID) and HSA (SG), among 11 authorities. Its most recent recorded inspection, by US FDA, closed on 30 September 2021 as VAI.

active US DMFs

valid CEPs

registered plants 1 with an FDA FEI number

1,215

filings across 39 regulators

These figures were checked against the regulators' own files on 25 July 2026

Plants

1 of 1 confirmed

Inspections

6 of 6 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

30 September 2021 VAI US FDA
23 August 2019 VAI US FDA
27 January 2017 VAI US FDA
11 November 2014 VAI US FDA
26 October 2012 VAI US FDA
19 November 2010 VAI US FDA

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

Registered plants

Site	FDA FEI
Jesenice u Prahy, United Arab Emirates	Not on file
Kiel, United Arab Emirates	Not on file
252 42 Vestec u Prahy, United Arab Emirates	Not on file
São Paulo, Brazil	Not on file
SAO PAULO, Brazil	Not on file
Baar, Switzerland	Not on file

6 further sites are on record.

Filings and GMP by regulator

Regulator	Filings	GMP certificates
Health Canada	107	None
MHRA (UK)	106	None
EMA	98	1
ANVISA (Brazil)	70	2
MPA (SE)	56	None
INFARMED (PT)	54	None
ZLG (DE)	None	6
BPOM (ID)	None	6
HSA (SG)	None	4
COFEPRIS (MX)	None	2
NAFDAC (NG)	None	2
NCELS (KZ)	None	2
CDSCO (India)	None	2
FDA (GH)	None	1
MINPROMTORG (RU)	None	1

Questions about Ferring

Does Ferring hold a US DMF or a CEP?

No active US drug master file or valid CEP is on record for Ferring. It does have 1,215 filings with 39 regulators, so it is registered, just not with the two strong registers buyers usually screen on.

Is Ferring FDA-registered?

One site operated by Ferring 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 Ferring's last inspection go?

The most recent inspection on record closed on 30 September 2021 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 6 inspections are on file.

Where does Ferring manufacture?

12 registered sites are on record, in United Arab Emirates, Brazil, Switzerland and Germany (Jesenice U Prahy, Kiel and 252 42 Vestec U Prahy among others). Every site is listed on this page with the register it came from.

Which regulators recognise Ferring's GMP?

Current GMP certificates are on record from ZLG (DE), BPOM (ID), HSA (SG), ANVISA (Brazil), COFEPRIS (MX) and 6 more. 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 30 September 2021.

Comparable suppliers

AESICA Pharmaceuticals also in Germany Alfred E. Tiefenbacher (GmbH also in Germany Almirall Hermal also in Germany Aqvida also in Germany Aristo Pharma also in Germany

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