Suppliers / Casen Recordati, S.L

Casen Recordati, S.L

Spain Updated 9 July 2026

Casen Recordati, S.L is a finished-dose manufacturer based in Spain. It appears in 1,081 regulatory filings across 23 regulators, without an active US DMF or CEP on file. Its filings concentrate with INFARMED (PT), EMA and AIFA (IT). Its GMP standing is certified by EMA, INFARMED (PT) and AEMPS (ES).

0
active US DMFs
0
valid CEPs
12
registered plants
1,081
filings across 23 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
Utebo, United Arab Emirates Not on file
Basel, Switzerland Not on file
Basel Town, Switzerland Not on file
Zaragoza, Spain Not on file
Utebo, Spain Not on file
Terrugem - Vila Verde, Portugal Not on file

6 further sites are on record.

Filings and GMP by regulator

Regulator Filings GMP certificates
INFARMED (PT) 296 2
EMA 177 2
AIFA (IT) 123 None
SWISSMEDIC (CH) 87 None
AEMPS (ES) 83 1
FAMHP (BE) 78 None

Questions about Casen Recordati, S.L

Does Casen Recordati, S.L hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Casen Recordati, S.L. It does have 1,081 filings with 23 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Casen Recordati, S.L manufacture?
12 registered sites are on record, in United Arab Emirates, Switzerland, Spain and Portugal (Utebo, Basel and Basel Town among others). Every site is listed on this page with the register it came from.
Which regulators recognise Casen Recordati, S.L's GMP?
Current GMP certificates are on record from EMA, INFARMED (PT) and AEMPS (ES). 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