Suppliers / ACE Pharmaceuticals

ACE Pharmaceuticals

Netherlands Updated 9 July 2026

ACE Pharmaceuticals is a finished-dose manufacturer based in Netherlands. It appears in 242 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with PPB (KE), EMA and FAMHP (BE). Its GMP standing is certified by EMA.

0
active US DMFs
0
valid CEPs
1
registered plants
242
filings across 6 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
Zeewolde, Netherlands Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
PPB (KE) 168 None
EMA 47 2
FAMHP (BE) 10 None
MPA (SE) 9 None
DMP (NO) 7 None
ZAMRA (ZM) 1 None

Questions about ACE Pharmaceuticals

Does ACE Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for ACE Pharmaceuticals. It does have 242 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does ACE Pharmaceuticals manufacture?
1 registered site is on record, in Netherlands (Zeewolde). Every site is listed on this page with the register it came from.
Which regulators recognise ACE Pharmaceuticals'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

Abbott Biologicals also in Netherlands Delpharm Meppel also in Netherlands Dsm Anti Infectives also in Netherlands Eurodrug Laboratories also in Netherlands N.V. Organon; also in Netherlands

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