Suppliers / Pharmasynthese

Pharmasynthese

France Updated 9 July 2026

Pharmasynthese is an API manufacturer based in France. Its GMP standing is certified by ANSM (FR).

0
active US DMFs
0
valid CEPs
2
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
SAINT PIERRE LES ELBEUF, France Not on file
Saint-Pierre-Les-Elbeuf, France Not on file

What they file, and where

Molecule Regulators Docs
Nefopam SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Nefopam API

Filings and GMP by regulator

Regulator Filings GMP certificates
ANSM (FR) None 18

Questions about Pharmasynthese

Where does Pharmasynthese manufacture?
2 registered sites are on record, in France (Saint Pierre LES Elbeuf and Saint-pierre-les-elbeuf). Every site is listed on this page with the register it came from.
What does Pharmasynthese make?
1 molecule is on record against Pharmasynthese, including Nefopam. Each links through to that molecule's full manufacturer list.
Which regulators recognise Pharmasynthese's GMP?
Current GMP certificates are on record from ANSM (FR). 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