Suppliers / Genus Pharmaceuticals

Genus Pharmaceuticals

United Kingdom 20 employees Updated 9 July 2026

Genus Pharmaceuticals is a finished-dose manufacturer based in United Kingdom. It appears in 160 regulatory filings across 2 regulators, without an active US DMF or CEP on file. Its filings concentrate with EMA and MHRA (UK). Its GMP standing is certified by MHRA (UK).

0
active US DMFs
0
valid CEPs
1
registered plants
160
filings across 2 regulators

Registered plants

Site FDA FEI
HUDDERSFIELD, United Kingdom Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 83 None
MHRA (UK) 77 2

Questions about Genus Pharmaceuticals

Does Genus Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Genus Pharmaceuticals. It does have 160 filings with 2 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Genus Pharmaceuticals manufacture?
1 registered site is on record, in United Kingdom (Huddersfield). Every site is listed on this page with the register it came from.
Which regulators recognise Genus Pharmaceuticals's GMP?
Current GMP certificates are on record from MHRA (UK). 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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Comparable suppliers

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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
EudraGMDP and national regulators
GMP certificates