Suppliers / Delpharm Poznan

Delpharm Poznan

Poland 189 employees Updated 9 July 2026

Delpharm Poznan is a finished-dose manufacturer based in Poland. It appears in 60 regulatory filings across 7 regulators, without an active US DMF or CEP on file. Its filings concentrate with EDE (AE), NCELS (KZ) and INVIMA (CO). Its GMP standing is certified by NAFDAC (NG) and EMA.

0
active US DMFs
0
valid CEPs
2
registered plants
60
filings across 7 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
Poznan, United Arab Emirates Not on file
Poznan, Poland Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EDE (AE) 20 None
NCELS (KZ) 16 None
INVIMA (CO) 8 None
MINSA (CR) 6 None
NPRA (MY) 5 None
ARCSA (EC) 3 None
NAFDAC (NG) None 1
EMA None 1

Questions about Delpharm Poznan

Does Delpharm Poznan hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Delpharm Poznan. It does have 60 filings with 7 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Delpharm Poznan manufacture?
2 registered sites are on record, in United Arab Emirates and Poland (Poznan among others). Every site is listed on this page with the register it came from.
Which regulators recognise Delpharm Poznan's GMP?
Current GMP certificates are on record from NAFDAC (NG) 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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Sources on this page

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