Suppliers / Aesica Queenborough

Aesica Queenborough

United Kingdom Updated 9 July 2026

Aesica Queenborough is an API and finished-dose manufacturer based in United Kingdom. It holds one active US drug master file. Its filings concentrate with MINSA (CR), NAFDAC (NG) and DIGEMAPS (DO). Its GMP standing is certified by MFDS (Korea), NAFDAC (NG) and ANVISA (Brazil).

1
active US DMFs
0
valid CEPs
1
registered plants
12
filings across 5 regulators

Registered plants

Site FDA FEI
QUEENBOROUGH, United Kingdom Not on file

What they file, and where

Molecule Regulators Docs
Isoflurane US FDA 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 6 None
NAFDAC (NG) 2 1
DIGEMAPS (DO) 2 None
FDA (GH) 1 None
NPRA (MY) 1 None
MFDS (Korea) None 2
ANVISA (Brazil) None 1

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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