Suppliers / Ashland Industries Europe

Ashland Industries Europe

Switzerland Updated 9 July 2026

Ashland Industries Europe is an API manufacturer based in Switzerland. It holds 4 valid CEPs across a filed portfolio of 3 molecules.

0
active US DMFs
4
valid CEPs
1
registered plants
2
filings across 1 regulators

Registered plants

Site FDA FEI
Schaffhausen, Switzerland Not on file

What they file, and where

Molecule Regulators Docs
Povidone EDQM 2
Copovidone EDQM 1
Povidone-Iodine EDQM 1

Also appears on these molecule pages

Povidone-Iodine API

Filings and GMP by regulator

Regulator Filings GMP certificates
EEC_EAEU 2 None

Questions about Ashland Industries Europe

Does Ashland Industries Europe hold a US DMF or a CEP?
Ashland Industries Europe holds 4 valid CEPs. 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 Ashland Industries Europe manufacture?
1 registered site is on record, in Switzerland (Schaffhausen). Every site is listed on this page with the register it came from.
What does Ashland Industries Europe make?
3 molecules are on record against Ashland Industries Europe, including Povidone, Copovidone and Povidone-Iodine. Each links through to that molecule's full manufacturer list.
Where does Ashland Industries Europe file?
Filings are on record with EEC (Eurasian Economic Union), 2 in total.

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