Suppliers / E-Pharma Trento

E-Pharma Trento

Italy 126 employees Updated 9 July 2026

E-Pharma Trento is a contract manufacturer based in Italy. It appears in 17 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with EEC_EAEU, DIGEMAPS (DO) and MINSA (CR). Its GMP standing is certified by EMA.

0
active US DMFs
0
valid CEPs
5
registered plants
17
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
Trento, United Arab Emirates Not on file
Trento, United Arab Emirates Not on file
Trento, Italy Not on file
38123 TRENTO, Italy Not on file
TRENTO, Italy Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EEC_EAEU 5 None
DIGEMAPS (DO) 5 None
MINSA (CR) 3 None
EDE (AE) 2 None
ARCSA (EC) 1 None
INVIMA (CO) 1 None
EMA None 1

Questions about E-Pharma Trento

Does E-Pharma Trento hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for E-Pharma Trento. It does have 17 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does E-Pharma Trento manufacture?
5 registered sites are on record, in United Arab Emirates and Italy (Trento, 38123 Trento and Trento among others). Every site is listed on this page with the register it came from.
Which regulators recognise E-Pharma Trento'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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Sources on this page

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