Suppliers / Ipc Process Center Gmbh And

Ipc Process Center Gmbh And

Germany Updated 9 July 2026

Ipc Process Center Gmbh And is an API manufacturer based in Germany. It holds one active US drug master file. Its GMP standing is certified by ZLG (DE) and EMA.

1
active US DMFs
0
valid CEPs
2
registered plants
0
filings across 0 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
Dresden, Germany Not on file
Sachsen, Germany Not on file

What they file, and where

Molecule Regulators Docs
Ibuprofen US FDA 1

Also appears on these molecule pages

Ibuprofen API

Filings and GMP by regulator

Regulator Filings GMP certificates
ZLG (DE) None 6
EMA None 1

Questions about Ipc Process Center Gmbh And

Does Ipc Process Center Gmbh And hold a US DMF or a CEP?
Ipc Process Center Gmbh And holds 1 active US drug master file. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Where does Ipc Process Center Gmbh And manufacture?
2 registered sites are on record, in Germany (Dresden and Sachsen). Every site is listed on this page with the register it came from.
What does Ipc Process Center Gmbh And make?
1 molecule is on record against Ipc Process Center Gmbh And, including Ibuprofen. Each links through to that molecule's full manufacturer list.
Which regulators recognise Ipc Process Center Gmbh And's GMP?
Current GMP certificates are on record from 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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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