Suppliers / Ever Pharma Jena

Ever Pharma Jena

Germany 76 employees Updated 9 July 2026

Ever Pharma Jena is a finished-dose manufacturer based in Germany. It appears in 42 regulatory filings across 7 regulators, without an active US DMF or CEP on file. Its filings concentrate with EDE (AE), JFDA (JO) and MINSA (CR). Its GMP standing is certified by ZLG (DE), MFDS (Korea) and EMA, among 4 authorities.

0
active US DMFs
0
valid CEPs
5
registered plants 1 with an FDA FEI number
42
filings across 7 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Jena, United Arab Emirates Not on file
Thueringen, United Arab Emirates Not on file
JENA, Germany Not on file
Thuringia, Germany Not on file
Germany, Germany 3032555054

Filings and GMP by regulator

Regulator Filings GMP certificates
EDE (AE) 14 None
JFDA (JO) 7 None
MINSA (CR) 6 None
INVIMA (CO) 5 None
UZPHARM (UZ) 5 None
ARCSA (EC) 4 None
ZLG (DE) None 6
MFDS (Korea) None 2
EMA None 1
ANVISA (Brazil) None 1

Questions about Ever Pharma Jena

Does Ever Pharma Jena hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Ever Pharma Jena. It does have 42 filings with 7 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Ever Pharma Jena FDA-registered?
One site operated by Ever Pharma Jena carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
Where does Ever Pharma Jena manufacture?
5 registered sites are on record, in United Arab Emirates and Germany (Jena, Thueringen and Jena among others). Every site is listed on this page with the register it came from.
Which regulators recognise Ever Pharma Jena's GMP?
Current GMP certificates are on record from ZLG (DE), MFDS (Korea), EMA and ANVISA (Brazil). 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