Suppliers / Weleda

Weleda

Brazil Updated 9 July 2026

Weleda is a finished-dose manufacturer based in Brazil. It appears in 727 regulatory filings across 9 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA, ANSM (FR) and ANVISA (Brazil). Its GMP standing is certified by ZLG (DE), EMA and ANSM (FR), among 4 authorities.

0
active US DMFs
0
valid CEPs
5
registered plants
727
filings across 9 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
São Paulo, Brazil Not on file
SAO PAULO, Brazil Not on file
Arlesheim, Switzerland Not on file
Schwaebisch Gmuend, Germany Not on file
HUNINGUE, France Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 235 3
ANSM (FR) 225 2
ANVISA (Brazil) 118 2
SWISSMEDIC (CH) 47 None
DMP (NO) 44 None
MEDSAFE (NZ) 42 None
ZLG (DE) None 8

Questions about Weleda

Does Weleda hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Weleda. It does have 727 filings with 9 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Weleda manufacture?
5 registered sites are on record, in Brazil, Switzerland, Germany and France (São Paulo, SAO Paulo and Arlesheim among others). Every site is listed on this page with the register it came from.
Which regulators recognise Weleda's GMP?
Current GMP certificates are on record from ZLG (DE), EMA, ANSM (FR) and ANVISA (Brazil). 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.

Comparing suppliers?

Choose your molecules and target markets. Weleda comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates