Suppliers / Laboratorios Reig Jofre

Laboratorios Reig Jofre

Spain 873 employees Updated 9 July 2026

Laboratorios Reig Jofre is a finished-dose manufacturer based in Spain. It appears in 52 regulatory filings across 7 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA, MHRA (UK) and DKMA (DK).

0
active US DMFs
0
valid CEPs
0
registered plants
52
filings across 7 regulators

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 33 None
MHRA (UK) 12 None
DKMA (DK) 2 None
EDA (EG) 2 None
DIGEMAPS (DO) 1 None
MINSA (CR) 1 None

Limited public record

Beyond the filing counts above, the public registers hold no plant, inspection or portfolio detail for this company as at 9 July 2026. We report that as a gap rather than inferring an answer.

Questions about Laboratorios Reig Jofre

Does Laboratorios Reig Jofre hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Laboratorios Reig Jofre. It does have 52 filings with 7 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Laboratorios Reig Jofre file?
Filings are on record with EMA, MHRA (UK), DKMA (DK), EDA (EG) and 3 other regulators, 52 in total.

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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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability