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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Sources on this page

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