Suppliers / Anhui Apeloa Biotechnology

Anhui Apeloa Biotechnology

China Updated 9 July 2026

Anhui Apeloa Biotechnology is an API manufacturer based in China. It holds one valid CEP. Its GMP standing is certified by EMA.

0
active US DMFs
1
valid CEPs
2
registered plants
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Dongzhi County, China Not on file
Dongzhi, China Not on file

What they file, and where

Molecule Regulators Docs
Colistin EDQM 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA None 1

Questions about Anhui Apeloa Biotechnology

Does Anhui Apeloa Biotechnology hold a US DMF or a CEP?
Anhui Apeloa Biotechnology holds 1 valid CEP. 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 Anhui Apeloa Biotechnology manufacture?
2 registered sites are on record, in China (Dongzhi County and Dongzhi). Every site is listed on this page with the register it came from.
What does Anhui Apeloa Biotechnology make?
1 molecule is on record against Anhui Apeloa Biotechnology, including Colistin. Each links through to that molecule's full manufacturer list.
Which regulators recognise Anhui Apeloa Biotechnology's GMP?
Current GMP certificates are on record from EMA. 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