Suppliers / Laboratorio Farmaceutico S.I.T. - Specialita Igienico Terapeutiche

Laboratorio Farmaceutico S.I.T. - Specialita Igienico Terapeutiche

Italy 2 employees Updated 9 July 2026

Laboratorio Farmaceutico S.I.T. - Specialita Igienico Terapeutiche is a finished-dose manufacturer based in Italy. It appears in 176 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with AIFA (IT), EMA and EDE (AE). Its GMP standing is certified by EMA.

0
active US DMFs
0
valid CEPs
7
registered plants
176
filings across 5 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
Tavernerio, United Arab Emirates Not on file
TAVERNERIO, Italy Not on file
MEDE, Italy Not on file
TAVERNERIO, Italy Not on file
MEDE, Italy Not on file
Tavernerio, Italy Not on file

1 further sites are on record.

Filings and GMP by regulator

Regulator Filings GMP certificates
AIFA (IT) 88 None
EMA 85 2
EDE (AE) 1 None
MINSA (CR) 1 None
UZPHARM (UZ) 1 None

Questions about Laboratorio Farmaceutico S.I.T. - Specialita Igienico Terapeutiche

Does Laboratorio Farmaceutico S.I.T. - Specialita Igienico Terapeutiche hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorio Farmaceutico S.I.T. - Specialita Igienico Terapeutiche. It does have 176 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorio Farmaceutico S.I.T. - Specialita Igienico Terapeutiche manufacture?
7 registered sites are on record, in United Arab Emirates and Italy (Tavernerio, Tavernerio and Mede among others). Every site is listed on this page with the register it came from.
Which regulators recognise Laboratorio Farmaceutico S.I.T. - Specialita Igienico Terapeutiche'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