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

Questions about Aesica Queenborough

Does Aesica Queenborough hold a US DMF or a CEP?
Aesica Queenborough holds 1 active US drug master file. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Where does Aesica Queenborough manufacture?
1 registered site is on record, in United Kingdom (Queenborough). Every site is listed on this page with the register it came from.
What does Aesica Queenborough make?
1 molecule is on record against Aesica Queenborough, including Isoflurane. Each links through to that molecule's full manufacturer list.
Which regulators recognise Aesica Queenborough's GMP?
Current GMP certificates are on record from MFDS (Korea), NAFDAC (NG) and ANVISA (Brazil). 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