Suppliers / Adienne

Adienne

Italy Updated 9 July 2026

Adienne is a finished-dose manufacturer based in Italy. It appears in 64 regulatory filings across 11 regulators, without an active US DMF or CEP on file. Its filings concentrate with AIFA (IT), Health Canada and MPA (SE). Its GMP standing is certified by EMA and MINPROMTORG (RU).

0
active US DMFs
0
valid CEPs
4
registered plants 1 with an FDA FEI number
64
filings across 11 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
Lugano, Switzerland Not on file
CAPONAGO, Italy Not on file
Caponago, Italy Not on file
Italy, Italy 3012017626

Filings and GMP by regulator

Regulator Filings GMP certificates
AIFA (IT) 12 None
Health Canada 12 None
MPA (SE) 6 None
ANSM (FR) 6 None
FAMHP (BE) 6 None
SWISSMEDIC (CH) 6 None
EMA None 1
MINPROMTORG (RU) None 1

Comparing suppliers?

Choose your molecules and target markets. Adienne comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Sources on this page

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