Suppliers / Prasfarma, S.L

Prasfarma, S.L

Spain Updated 9 July 2026

Prasfarma, S.L is a contract manufacturer based in Spain. It appears in 9 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with JFDA (JO), EMA and AEMPS (ES). Its GMP standing is certified by EMA and ANVISA (Brazil).

0
active US DMFs
0
valid CEPs
2
registered plants
9
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
BARCELONA, Spain Not on file
Manlleu, Spain Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
JFDA (JO) 6 None
EMA 2 1
AEMPS (ES) 1 None
ANVISA (Brazil) None 1

Questions about Prasfarma, S.L

Does Prasfarma, S.L hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Prasfarma, S.L. It does have 9 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Prasfarma, S.L manufacture?
2 registered sites are on record, in Spain (Barcelona and Manlleu). Every site is listed on this page with the register it came from.
Which regulators recognise Prasfarma, S.L's GMP?
Current GMP certificates are on record from EMA 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.

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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