Suppliers / Denk Pharma GmbH

Denk Pharma GmbH

Germany 683 employees 3 duplicate records merged Updated 9 July 2026

Denk Pharma GmbH is a finished-dose manufacturer based in Germany. It appears in 536 regulatory filings across 15 regulators, without an active US DMF or CEP on file. Its filings concentrate with RAMA (GE), EFDA (ET) and EMA. Its GMP standing is certified by ZLG (DE), TMDA (TZ) and EMA, among 4 authorities.

0
active US DMFs
0
valid CEPs
6
registered plants
536
filings across 15 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
Tittmoning, United Arab Emirates Not on file
81675 Munchen, United Arab Emirates Not on file
Munich, Germany Not on file
Munich, Germany Not on file
Tittmoning, Germany Not on file
Bavaria, Germany Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
RAMA (GE) 109 None
EFDA (ET) 73 None
EMA 64 2
FDA (GH) 62 1
ZAMRA (ZM) 52 None
TMDA (TZ) 46 4
ZLG (DE) None 12

Questions about Denk Pharma GmbH

Does Denk Pharma GmbH hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Denk Pharma GmbH. It does have 536 filings with 15 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Denk Pharma GmbH manufacture?
6 registered sites are on record, in United Arab Emirates and Germany (Tittmoning, 81675 Munchen and Munich among others). Every site is listed on this page with the register it came from.
Which regulators recognise Denk Pharma GmbH's GMP?
Current GMP certificates are on record from ZLG (DE), TMDA (TZ), EMA and FDA (GH). 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