Suppliers / Zambon Switzerland

Zambon Switzerland

Switzerland Updated 9 July 2026

Zambon Switzerland is a finished-dose manufacturer based in Switzerland. It appears in 52 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with AEMPS (ES) and EMA. Its GMP standing is certified by EMA and AEMPS (ES).

0
active US DMFs
0
valid CEPs
3
registered plants
52
filings across 2 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
CADEMPINO, Switzerland Not on file
Barcelona, Spain Not on file
Santa Perpetua De Mogoda, Spain Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
AEMPS (ES) 34 1
EMA 18 3

Questions about Zambon Switzerland

Does Zambon Switzerland hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Zambon Switzerland. It does have 52 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Zambon Switzerland manufacture?
3 registered sites are on record, in Switzerland and Spain (Cadempino, Barcelona and Santa Perpetua De Mogoda). Every site is listed on this page with the register it came from.
Which regulators recognise Zambon Switzerland's GMP?
Current GMP certificates are on record from EMA 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