Suppliers / Horus Pharma

Horus Pharma

France 269 employees Updated 9 July 2026

Horus Pharma is a finished-dose manufacturer based in France. It appears in 136 regulatory filings across 11 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA, EDA (EG) and ANSM (FR). Its GMP standing is certified by EDA (EG).

0
active US DMFs
0
valid CEPs
1
registered plants
136
filings across 11 regulators

Registered plants

Site FDA FEI
Nyon, Switzerland Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 73 None
EDA (EG) 18 2
ANSM (FR) 18 None
FAMHP (BE) 8 None
AEMPS (ES) 8 None
MPA (SE) 4 None

Questions about Horus Pharma

Does Horus Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Horus Pharma. It does have 136 filings with 11 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Horus Pharma manufacture?
1 registered site is on record, in Switzerland (Nyon). Every site is listed on this page with the register it came from.
Which regulators recognise Horus Pharma's GMP?
Current GMP certificates are on record from EDA (EG). 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