Suppliers / Sag Manufacturing S.L.U

Sag Manufacturing S.L.U

Spain 2 duplicate records merged Updated 9 July 2026

Sag Manufacturing S.L.U is a finished-dose manufacturer based in Spain. It appears in 45 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with ARCSA (EC), MINSA (CR) and COFEPRIS (MX). Its GMP standing is certified by ANVISA (Brazil), NAFDAC (NG) and EMA, among 4 authorities.

0
active US DMFs
0
valid CEPs
4
registered plants
45
filings across 6 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
Madrid, United Arab Emirates Not on file
Madrid, Spain Not on file
MADRID, Spain Not on file
San Agustin Del Guadalix, Spain Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ARCSA (EC) 16 None
MINSA (CR) 11 None
COFEPRIS (MX) 10 None
BOMRA (BW) 5 None
UZPHARM (UZ) 2 None
JFDA (JO) 1 None
ANVISA (Brazil) None 4
NAFDAC (NG) None 1
EMA None 1
AEMPS (ES) None 1

Questions about Sag Manufacturing S.L.U

Does Sag Manufacturing S.L.U hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Sag Manufacturing S.L.U. It does have 45 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Sag Manufacturing S.L.U manufacture?
4 registered sites are on record, in United Arab Emirates and Spain (Madrid, Madrid and San Agustin Del Guadalix among others). Every site is listed on this page with the register it came from.
Which regulators recognise Sag Manufacturing S.L.U's GMP?
Current GMP certificates are on record from ANVISA (Brazil), NAFDAC (NG), EMA and AEMPS (ES). 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