Suppliers / Vifor Pharma

Vifor Pharma

Switzerland Updated 9 July 2026

Vifor Pharma is a finished-dose manufacturer based in Switzerland. It appears in 49 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with DKMA (DK), AEMPS (ES) and TGA (Australia). Its GMP standing is certified by ZLG (DE) and CDSCO (India).

0
active US DMFs
0
valid CEPs
3
registered plants
49
filings across 6 regulators

Registered plants

Site FDA FEI
Munich, Germany Not on file
sector ii kandla special economic zone, India Not on file
Terrugem, Portugal Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DKMA (DK) 20 None
AEMPS (ES) 14 None
TGA (Australia) 6 None
US FDA 4 None
INFARMED (PT) 3 None
MHRA (UK) 2 None
ZLG (DE) None 2
CDSCO (India) None 2

Questions about Vifor Pharma

Does Vifor Pharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Vifor Pharma. It does have 49 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Vifor Pharma manufacture?
3 registered sites are on record, in Germany, India and Portugal (Munich, Sector Ii Kandla Special Economic Zone and Terrugem). Every site is listed on this page with the register it came from.
Which regulators recognise Vifor Pharma's GMP?
Current GMP certificates are on record from ZLG (DE) and CDSCO (India). 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