Suppliers / Ivf Hartmann A G

Ivf Hartmann A G

Switzerland Updated 9 July 2026

Ivf Hartmann A G is a finished-dose manufacturer based in Switzerland. It appears in 5 regulatory filings across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by EMA.

0
active US DMFs
0
valid CEPs
1
registered plants
5
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Neuhausen am Rheinfall, Switzerland Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
SWISSMEDIC (CH) 5 None
EMA None 1

Questions about Ivf Hartmann A G

Does Ivf Hartmann A G hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Ivf Hartmann A G. It does have 5 filings with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Ivf Hartmann A G manufacture?
1 registered site is on record, in Switzerland (Neuhausen Am Rheinfall). Every site is listed on this page with the register it came from.
Which regulators recognise Ivf Hartmann A G's GMP?
Current GMP certificates are on record from 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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Comparable suppliers

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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