Suppliers / Servier Laboratories

Servier Laboratories

United Kingdom 2 duplicate records merged Updated 9 July 2026

Servier Laboratories is a finished-dose manufacturer based in United Kingdom. It appears in 244 regulatory filings across 10 regulators, without an active US DMF or CEP on file. Its filings concentrate with SAHPRA (ZA), NMRC (NA) and MEDSAFE (NZ). Its GMP standing is certified by NAFDAC (NG).

0
active US DMFs
0
valid CEPs
1
registered plants
244
filings across 10 regulators

Registered plants

Site FDA FEI
Paris, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
SAHPRA (ZA) 116 None
NMRC (NA) 40 None
MEDSAFE (NZ) 24 None
MHRA (UK) 19 None
ARCSA (EC) 19 None
MINSA (CR) 13 None
NAFDAC (NG) None 2

Questions about Servier Laboratories

Does Servier Laboratories hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Servier Laboratories. It does have 244 filings with 10 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Servier Laboratories manufacture?
1 registered site is on record, in Nigeria (Paris). Every site is listed on this page with the register it came from.
Which regulators recognise Servier Laboratories's GMP?
Current GMP certificates are on record from NAFDAC (NG). 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