Suppliers / Delpharm Reims

Delpharm Reims

France 166 employees Updated 9 July 2026

Delpharm Reims is a finished-dose manufacturer based in France. It appears in 24 regulatory filings across 8 regulators, without an active US DMF or CEP on file. Its filings concentrate with EDE (AE), ARCSA (EC) and MINSA (CR). Its GMP standing is certified by ANSM (FR), ANVISA (Brazil) and EMA.

0
active US DMFs
0
valid CEPs
2
registered plants
24
filings across 8 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
51100 reims, United Arab Emirates Not on file
REIMS, France Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EDE (AE) 10 None
ARCSA (EC) 6 None
MINSA (CR) 3 None
NAFDAC (NG) 1 None
NPRA (MY) 1 None
NCELS (KZ) 1 None
ANSM (FR) None 8
ANVISA (Brazil) None 2
EMA None 2

Scale

Year Revenue Exports Destinations
2024 $94.0M Not reported Not reported

Export figures are customs aggregates. We do not publish the identity of any buyer. Revenue shown in US dollars, converted from the reported currency.

Questions about Delpharm Reims

Does Delpharm Reims hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Delpharm Reims. It does have 24 filings with 8 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Delpharm Reims manufacture?
2 registered sites are on record, in United Arab Emirates and France (51100 Reims and Reims). Every site is listed on this page with the register it came from.
Which regulators recognise Delpharm Reims's GMP?
Current GMP certificates are on record from ANSM (FR), ANVISA (Brazil) and EMA. 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
Company filings
Revenue as reported