Suppliers / Drossapharm

Drossapharm

Switzerland 74 employees Updated 9 July 2026

Drossapharm is a finished-dose manufacturer based in Switzerland. It appears in 211 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with SWISSMEDIC (CH), EMA and EDE (AE). Its GMP standing is certified by EMA.

0
active US DMFs
0
valid CEPs
3
registered plants
211
filings across 3 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
Birsweg 1, United Arab Emirates Not on file
Basel, Switzerland Not on file
Arlesheim, Switzerland Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
SWISSMEDIC (CH) 182 None
EMA 27 1
EDE (AE) 2 None

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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